Preformation and neoformation in shoots of Nothofagus antarctica (G. Forster) Oerst. (Nothofagaceae) shrubs from northern Patagonia

The size (length and diameter) and number of leaf primordia of winter buds of Nothofagus antarctica (G. Forster) Oerst. shrubs were compared with the size and number of leaves of shoots derived from buds in equivalent positions. Buds developed in two successive years were compared in terms of size and number of leaf primordia. Bud size and the number of leaf primordia per bud were greater for distal than for proximally positioned buds. Shoots that developed in the five positions closest to the distal end of their parent shoots had significantly more leaves than more proximally positioned shoots of the same parent shoots. The positive relationship between the size of a shoot and that of its parent shoot was stronger for proximal than for distal positions on the parent shoots. For each bud position on the parent shoots there were differences in the number of leaf primordia per bud between consecutive years. The correlations between the number of leaf primordia per bud and bud size, bud position and parent shoot size varied between years. Only shoots produced close to the distal end of a parent shoot developed neoformed leaves; more proximal sibling shoots consisted entirely of preformed leaves. Leaf neoformation, a process usually linked with high shoot vigour in woody plants, seems to be widespread among the relatively small shoots developed in N. antarctica shrubs, which may relate to the species' opportunistic response to disturbance.     

RADIATION DAMAGE IN APPLE SHOOT APICES

Pratt , Charlotte , John Einset , and Mohammad Zahur . (N. Y. S. Agric. Expt. Sta., Geneva.) Radiation damage in apple shoot apices. Amer. Jour. Bot. 46(7): 537–544. Illus. 1959.—Pattern of shoot growth and anatomy of the shoot apex of ‘Golden Delicious’ apple trees on ‘East Malling IX’ rootstock are compared in normal trees and those growing under chronic gamma irradiation (average doses of 17–48 r per 20-hr. day) at Brookhaven National Laboratory. Bud damage in 6 varieties of apple trees is compared. Irradiated ‘Golden Delicious’ formed lateral buds on the current year's shoot, but the following year these buds grew into spurs which failed to form a terminal bud (“budless” spurs) and enlarged to form “club tips” and “swollen spurs” in this and subsequent years. Cells with thick walls and lightly stained cytoplasm occurred in shoot apices of irradiated lateral buds in mid-June. The first tunica layer was more resistant to radiation than the inner tunica layers and the corpus; pith rib meristem was still more resistant. Inflorescence and floral meristems were rarely found, but once formed, continued development. One-year-old budless spurs had a few leaves but neither an organized apical meristem nor leaf primordia. Surface of the apex was often folded. Periderm and, later, deep-lying wound cambium developed. Expansion of pith, vascular tissue, cortex, wound cambium and periderm caused enlargement of club tips and swollen spurs. Many lateral buds from the gamma field which were propagated without irradiation in early August grew into long shoots with terminal buds. Scions removed from irradiation in November and inserted into normal trees showed lower survival and many of their shoots were budless. This suggests that the capacity for normal growth of a bud damaged by chronic irradiation is greater in mid-summer than later in the year. With reference to percentage of budless shoots, ‘Delicious,’ ‘Golden Delicious’ and ‘McIntosh’ were more sensitive to an average dose of 24 r per day and lower doses than were ‘Cox,’ ‘Macoun’ and ‘Spy.’ Symptoms of radiation damage in apple buds during the first year were similar following acute or chronic irradiation. Degree of radiation damage, as expressed by death of apical meristems, was concluded to vary with stage of development of the bud, structure of the apical meristem, and genetic constitution.     

The Morphogenesis of Apple Buds: III. The Inception of Flowers

The early stages in the change from vegetative to reproductivedevelopment of apple spur terminal buds were followed by dissectionof buds from untreated trees, and from trees defoliated at differenttimes in the season. A change in the development of the leafprimordia occurred when there were approximately eight in thebud. This was followed by the development of bracts, which appearedto be necessary for the formation of actual flower parts. Leafprimordia tend to inhibit this process. Whereas their effectupon the apical meristem was subsequently reduced by the formationof bracts, so that eventually a terminal flower formed, theireffect upon the lower lateral meristems was unaltered. Thesemeristems therefore remained in a vegetative state. In addition to the number of leaf primordia in the bud, thedegree of dormancy may be an important factor in determiningthe onset of flowering. Since the number of leaf primordia invegetative buds at the end of the season is eight, the spatialdistribution of primordia on the main axis of the bud and theirvascular connexions might have a decisive effect on bud development.This was related to the effect of older primordia in the budupon the development of younger ones. In buds in which theseolder primordia were inhibited by foliage, etc., i.e. thosewith a long plastochrone, no effects were observed upon thedevelopment of younger primordia and the buds remained vegetative. Whilst correlative inhibition of buds thus affected their abilityto form flowers, there is no evidence of a critical leaf areafor flowering. Flowering in apple buds is more likely to bedue to the removal of factors inhibiting reproductive developmentthan to the synthesis of a specific flower inducing substanceas such.     

Bud Content and its Relation to Shoot Size and Structure in Nothofagus pumilio(Poepp. et Endl.) Krasser (Nothofagaceae)

Buds of shoots from the trunk, main branches, secondary branchesand short branches of 10–21 year-old Nothofagus pumiliotrees were dissected and their contents recorded. The numberof differentiated nodes in buds was compared with the numberof nodes of sibling shoots developed at equivalent positionsduring the following growing season. Axillary buds generallyhad four cataphylls, irrespective of bud position in the tree,whereas terminal buds had up to two cataphylls. There were morenodes in terminal buds, and the most distal axillary buds, oftrunk shoots than in more proximal buds of trunk shoots, andin all buds of shoots at all other positions. The highest numberof nodes in the embryonic shoot of a bud varied between 15 and20. All shoots had proximal lateral buds containing an embryonicshoot with seven nodes, four with cataphylls and three withgreen leaf primordia. The largest trunk, and main branch, shootswere made up of a preformed portion and a neoformed portion;all other shoots were entirely preformed. In N. pumilio, theacropetally-increasing size of the sibling shoots derived froma particular parent shoot resulted from differences in: (1)the number of differentiated organs in the buds; (2) the probabilityof differentiation of additional organs during sibling shootextension; (3) sibling shoot length; (4) sibling shoot diameter;and (5) the death of the apex and the most distal leaves ofeach sibling shoot. Copyright 2000 Annals of Botany Company Axis differentiation, branching, bud structure, leaf primordia, neoformation, Nothofagus pumilio, preformation, size gradient     

Development of shoot inHydrangea macrophylla I. Terminal and axillary buds

The structure of shoots, in particular of winter buds, ofHydrangea macrophylla was examined. The non-flower-bearing shoot is usually composed of a lower and an upper part, between which a boundary is discernible by means of a distinctly short internode. This internode is the lowermost of the upper part, and it is usually shorter than the internodes immediately above and below, although the internodes tend to shorten successively from the proximal to the distal part of the shoot. Variations exist in the following characters among the terminal bud, the axillary bud on the lower part of the shoot and the axillary bud on the upper part: (1) length of bud; (2) character of the outermost pair of leaf primordia; (3) degree of development of secondary buds in the winter bud; and (4) the number of leaf primordia. Usually, the terminal bud contains several pairs of foliage leaf primordia with a primordial inflorescence at the terminal of the bud, but the axiallary bud contains only the primordia of foliage leaves in addition to a pair of bud scales.     

Development and Growth Potential of Axillary Buds in Roses as Affected by Bud Age

The effect of axillary bud age on the development and potentialfor growth of the bud into a shoot was studied in roses. Ageof the buds occupying a similar position on the plant variedfrom 'subtending leaf just unfolded' up to 1 year later. Withincreasing age of the axillary bud its dry mass, dry-matterpercentage and number of leaves, including leaf primordia, increased.The apical meristem of the axillary bud remained vegetativeas long as subjected to apical dominance, even for 1 year. The potential for growth of buds was studied either by pruningthe parent shoot above the bud, by grafting the bud or by culturingthe bud in vitro. When the correlative inhibition (i.e. dominationof the apical region over the axillary buds) was released, additionalleaves and eventually a flower formed. The number of additionalleaves decreased with increasing bud age and became more orless constant for axillary buds of shoots beyond the harvestablestage, while the total number of leaves preceding the flowerincreased. An increase in bud age was reflected in a greaternumber of scales, including transitional leaves, and in a greaternumber of non-elongated internodes of the subsequent shoot.Time until bud break slightly decreased with increasing budage; it was long, relatively, for 1 year old buds, when theysprouted attached to the parent shoot. Shoot length, mass andleaf area were not clearly affected by the age of the bud thatdeveloped into the shoot. With increasing bud age the numberof pith cells in the subsequent shoot increased, indicatinga greater potential diameter of the shoot. However, final diameterwas dependent on the assimilate supply after bud break. Axillarybuds obviously need a certain developmental stage to be ableto break. When released from correlative inhibition at an earlierstage, increased leaf initiation occurs before bud break.Copyright1994, 1999 Academic Press Age, axillary bud, cell number, cell size, pith, shoot growth, Rosa hybrida, rose     

Determination for inflorescence development is a stable state,separable from determination for flower development in Pisum sativum L. buds

Terminal meristems of Pisum sativum (garden pea) transit from vegetative to inflorescence development, and begin producing floral axillary meristems. Determination for inflorescence development was assessed by culturing excised buds and meristems. The first node of floral initiation (NFI) for bud expiants developing in culture and for adventitious shoots forming on cultured meristems was compared with the NFI of intact control buds. When terminal buds having eight leaf primordia were excised from plants of different ages (i.e., number of unfolded leaves) and cultured on 6-benzylaminopurine and kinetin-supplemented medium, the NFI was a function of the age of the source plant. By age 3, all terminal buds were determined for inflorescence development. Determination occurred at least eight nodes before the first axillary flower was initiated. Thus, the axillary meristems contributing to the inflorescence had not formed at the time the bud was explanted. Similar results were obtained for cultured axillary buds. In addition, meristems excised without leaf primordia from axillary buds three nodes above the cotyledons of age-3 plants gave rise to adventitious buds with an NFI of 8.3 ±0.3 nodes. In contrast seed-derived plants had an NFI of 16.5 ±0.2. Thus cells within the meristem were determined for inflorescence development. These findings indicate that determination for inflorescence development in P. sativum is a stable developmental state, separable from determination for flower development, and occurring prior to initiation of the inflorescence at the level of meristems.     

Periods of organogenesis in mono- and bicyclic annual shoots of Juglans regia L. (Juglandaceae)

The organogenetic cycle of shoots on main branches of 4-year-old Juglans regia trees was studied. Mono- and bicyclic floriferous and vegetative annual shoots were analysed. Five parent annual shoot types were sampled between October 1992 and August 1993. Organogenesis of summer growth units was monitored between 16 Jun. and 3 Aug. 1993. Variations over time in the number of nodes, cataphylls and embryonic green leaves of terminal buds were studied. The number of nodes of parent shoot buds was compared with the number of nodes of shoots derived from parent shoot buds. The spring growth units of mono- and bicyclic shoots consist exclusively of preformed leaves which were differentiated, respectively, during the spring flush of growth (mid-April until mid-May) or the summer flush of growth (mid-June until early August) in the previous growing season. Thus, winter buds may consist of flower and leaf primordia differentiated in two different periods during annual shoot extension. The summer growth units of bicyclic shoots consist of preformed leaves that were differentiated in spring buds during the spring flush of growth in the current growing season. Bud morphology is compared between spring and summer shoots.     

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     

Periods of organogenesis in shoots of Nothofagus dombeyi (Mirb.) oersted (Nothofagaceae)

The organogenetic cycle of main-branch shoots of Nothofagus dombeyi (Nothofagaceae) was studied. Twelve samples of 52-59 parent shoots were collected from a roadside population between September 1999 and October 2000. Variations over time in the number of nodes of terminal and axillary buds, and the length, diameter and number of leaves of shoots derived from these buds (sibling shoots) were analysed. The number of nodes of buds developed by parent shoots was compared with the number of nodes of buds developed, I year later, by sibling shoots. The length, diameter and number of leaves of sibling shoots increased from October 1999 to February 2000 in those shoots with a terminal bud. However, extension of most sibling shoots, including the first five most distal leaf primordia, ceased before February due to abscission of the shoot apex. Axillary buds located most distally on a shoot had more nodes than both terminal buds and more proximal axillary buds. The longest shoots included a preformed part and a neoformed part. The organogenetic event which initiated the neoformed organs continued until early autumn, giving rise to the following year's preformation. The absence of cataphylls in terminal buds could indicate a low intensity of shoot rest. The naked terminal bud of Nothofagus spp. could be interpreted as a structure less specialized than the scaled bud found in genera of Fagaceae and Betulaceae.     

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     

Correlation between development of female flower buds and expression of the CS-ACS2 gene in cucumber plants

Ethylene plays a key role in sex determination of cucumber flowers. Gynoecious cucumber shoots produce more ethylene than monoecious shoots. Because monoecious cucumbers produce both male and female flower buds in the shoot apex and because the relative proportions of male and female flowers vary due to growing conditions, the question arises as to whether the regulation of ethylene biosynthesis in each flower bud determines the sex of the flower. Therefore, the expression of a 1-aminocyclopropane-1-carboxylic acid synthase gene, CS-ACS2, was examined in cucumber flower buds at different stages of development. The results revealed that CS-ACS2 mRNA began to accumulate just beneath the pistil primordia of flower buds at the bisexual stage, but was not detected prior to the formation of the pistil primordia. In buds determined to develop as female flowers, CS-ACS2 mRNA continued to accumulate in the central region of the developing ovary where ovules and placenta form. In gynoecious cucumber plants that produce only female flowers, accumulation of CS-ACS2 mRNA was detected in all flower buds at the bisexual stage and at later developmental stages. In monoecious cucumber, flower buds situated on some nodes accumulated CS-ACS2 mRNA, but others did not. The proportion of male and female flowers in monoecious cucumbers varied depending on the growth conditions, but was correlated with changes in accumulation of CS-ACS2 mRNA in flower buds. These results demonstrate that CS-ACS2-mediated biosynthesis of ethylene in individual flower buds is associated with the differentiation and development of female flowers.     

Axillary meristems and the development of epicormic buds in wollemi pine (Wollemia nobilis)

Intact trees of Wollemia nobilis Jones, Hill and Allen (Araucariaceae) routinely develop multiple coppice shoots as well as orthotropic epicormic shoots that become replacement or additional leaders. As these are unusual architectural features for the Araucariaceae, an investigation was made of the axillary meristems of the main stem and their role in the production of epicormic and possibly coppice shoots. Leaf axils, excised from the apex to the base of 2-m-high W. nobilis plants (seedling origin, ex situ grown), were examined anatomically. Small, endogenous, undifferentiated (no leaf primordia, no vascular or provascular connections) meristems were found in the axils from near the shoot apex. In the more proximal positions about half the meristems sampled did not differentiate further, but became tangentially elongated to compensate for increases in stem diameter. In the remaining axils the meristems slowly developed into bud primordia, although these buds usually developed few leaf primordia and their apical 'domes' were wide and flat. Associated vascular development was generally restricted to provascular dedifferentiation of the cortical parenchyma, with the procambium usually forming a 'closed loop' that did not extend back to the secondary vascular tissues. Development of the meristems was very uneven with adjacent axils often at widely differing stages of development into buds. The study shows that, unlike most conifers, W. nobilis possesses long-lived meristematic potential in most, if not all, leaf axils. Unlike other araucarias that have been investigated, many of the meristems in the orthotropic main stem will slowly develop into bud primordia beneath the bark in intact plants. It appears likely that this slow but continued development provides a ready source of additional or replacement leaders and thus new branches and leaves.     

Dynamics of flower development and vegetative shoot growth in the high mountain plant Saxifraga bryoides L.

Saxifraga bryoides L. is an abundant species in the subnival and nival zone of the European mountains. First flowering occurs, at the earliest, 6 weeks after snowmelt. This is a remarkably long prefloration period in an environment with a short growing season. To gain more information about the developmental strategies of this species, the timing and the dynamics of flower bud formation and vegetative shoot growth were studied at sites with growing seasons of different lengths at two subnival locations (2650 and 2880 m a.s.l.) in the Tyrolean Alps. At an early, mid and late thawing site, individuals emerging from the winter snow were labelled. Reproductive and vegetative shoots were sampled at regular intervals throughout the growing season and analysed, using different microscopic techniques. Flower buds of S. bryoides develop in three cohorts. Provided the growing season is long enough, cohorts 1 and 2 come into flower, whereas cohort 3 buds remain primordial and continue to develop after winter. New flower primordia appear as day-length decreases from August on, which suggests a short-day requirement for floral initiation. At the end of the growing season, flower buds of different stages are present, but only primordial stages survive winter. Thus, flower buds of S. bryoides develop largely or even completely in the year of anthesis. Developmental dynamics were quite similar at the different sites. Time from flower initiation until anthesis took about 2 months, independently of whether flowers were formed within one or two seasons. All of the leaves on vegetative short-stem shoots turnover within a growing season. Leaves having passed winter continuously decline and are replaced by newly formed ones (21±3 at the mid-thawing site and 18±1 leaves at the short-season site). An individual leaf functions therefore, on average, about 12 months. In most years the seed crop of S. bryoides results mainly from the first cohort of flowers in an individual. In a changing climate with a prolonged growing season, the chance of two cohorts to develop mature seeds from flower cohorts 1 and 2 would increase.     

NODE COUNTING IN AXILLARY BUDS OF NICOTIANA TABACUM CV. WISCONSIN 38, A DAY-NEUTRAL PLANT

A mature, quiescent, primary axillary bud on the main axis of a flowering Nicotiana tabacum cv. Wisconsin 38 plant, when released from apical dominance and before forming its terminal flower, produced a number of nodes which was dependent upon its position on the main axis. Each bud produced about one more node than the next bud above it. The total number of nodes produced by an axillary bud was about 6 to 8 greater than the number of nodes present above this bud on the main axis. At anthesis of the terminal flower on the main axis, mature, quiescent, primary axillary buds had initiated 7 to 9 leaf primordia while secondary axillary buds, sometimes present in addition to the primary ones, had initiated 4 to 5 leaf primordia. When permitted to grow out independently, primary and secondary axillary buds located at the same node on the main axis produced the same number of nodes before forming their terminal flowers. In contrast, immature primary axillary buds which had produced only 5 leaf primordia and which were released from apical dominance prior to the formation of flowers on the main axis produced only as many nodes as would be produced above them on the main axis by the terminal meristem, i.e., “extra” nodes were not produced. Therefore, it is the physiological status of the plant and not the number of nodes on the bud at the time of release from apical dominance that influenced the node-counting process of a bud. When two axillary buds were permitted to develop on the same main axis, each produced the same number of nodes as single axillary buds developing at these nodes. Thus, the counting process in an axillary bud of tobacco is independent of other buds. Axillary buds on main axes of plants that had been placed horizontally produced the same number of nodes as identically-positioned axillary buds on vertical plants, indicating that gravity does not play a major role in the counting, by an axillary bud, of the nodes on the main axis.     

Growth Context and Fate of Axillary Meristems of Young Peach Trees. Influence of Parent Shoot Growth Characteristics and of Emergence Date

The relationship between several growth components of a shootand the fates of the axillary meristems (developing in the axilsof the leaves) borne by that shoot were studied, on first-ordershoots of young peach trees. A comprehensive picture of thoserelationships was obtained by a discriminant analysis. Shootgrowth at meristem emergence date was characterized by internodelength, leaf-production rate and leaf-unfolding duration. Allpossible fates of axillary meristems at the end of the growingseason (i.e. blind nodes, single vegetative or flower bud, budassociations, sylleptic or proleptic shoots) were considered.Shoot-elongation rate determined meristem fates quantitatively.The number of buds produced by a meristem increased when theshoot-elongation rate increased. Qualitatively, the fate of axillary meristems was related tothe balance between shoot-growth components. If the subtendingleaf unfolded slowly, sylleptic or proleptic shoots were morelikely to develop than bud associations, for high shoot-elongationrates; and flower buds were more frequent than vegetative buds,for low shoot-elongation rates. Compared to flower buds, blindnodes appeared for similar shoot-elongation rates but longerinternodes and lower leaf-production rates. The emergence dateslightly modified the relation between shoot growth and axillary-meristemfates, but the main features held true throughout the growingseason. The relationships between shoot growth and meristem fates mayresult from competitive interactions between the growing subtendingleaf and the developing axillary meristem. Growing conditionsmight also influence both shoot growth and meristem fates byfavouring either cell enlargement or cell division.Copyright1995, 1999 Academic Press Peach tree, Prunus persica (L.) Batsch, axillary meristem, meristem fate, branching, flowering, shoot growth, discriminant analysis, exploratory analysis     

DIFFERENTIATION OF LATERAL SHOOTS AS THORNS IN ULEX EUROPAEUS

Ulex europaeus is a much-branched shrub with small, narrow, spine-tipped leaves and axillary thorn shoots. The origin and development of axillary shoots was studied as a basis for understanding the changes that occur in the axillary shoot apex as it differentiates into a thorn. Axillary bud primordia are derived from detached portions of the apical meristem of the primary shoot. Bud primordia in the axils of juvenile leaves on seedlings develop as leafy shoots while those in the axils of adult leaves become thorns. A variable degree of vegetative development prior to thorn differentiation is exhibited among these secondary thorn shoots even on the same axis. Commonly the meristems of secondary axillary shoots initiate 3–9 bracteal leaves with tertiary axillary buds before differentiating as thorns. In other cases the meristems develop a greater number of leaves and tertiary buds as thorn differentiation is delayed. The initial stages in the differentiation of secondary shoot meristems as thorns are detected between plastochrons 10–20, depending on vigor of the parent shoot. A study of successive lateral buds on a shoot shows an abrupt conversion from vegetative development to thorn differentiation. The conversion involves the termination of meristematic activity of the apex and cessation of leaf initiation. Within the apex a vertical elongation of cells of the rib meristem initials and their immediate derivatives commences the attenuation of the apex which results in the pointed thorn. All cells of the apex elongate parallel to the axis and proceed to sclerify basipetally. Back of the apex some cortical cells in which cell division has persisted longer differentiate as chlorenchyma. Although no new leaves are initiated during the extension of the apex, provascular strands are present in the thorn tip. Fibrovascular bundles and bundles of cortical fibers not associated with vascular tissue differentiate in the thorn tip and are correlated in position with successive incipient leaves in the expected phyllotactic sequence, the more developed bundles being related to the first incipient leaves. Some secondary shoots displayed variable atypical patterns of meristem differentiation such as abrupt conversion of the apex resulting in sclerification with limited cell elongation and small, inhibited leaves. These observations raise questions concerning the nature of thorn induction and the commitment of meristems to thorns.     

Anatomical and Histochemical Changes of Norway Spruce Buds Induced by Simulated Acid Rain

The study was focused on changes of anatomical and histochemical parameters of buds of 4-year-old Norway spruce (Picea abies L. Karst) trees subjected to simulated acid rain (SAR). Solutions of pH 2.9 and 3.9 were applied by spraying on shoot and/or by watering for two years. No macroscopic changes of buds or needles were observed in connection with SAR application and the only induced change was 2-week earlier onset of bud break in all treated variants compared to the control. Two-year treatment caused decrease in number of leaf primordia and increase in number of living bud scales in treated dormant buds while these parameters remained unchanged in the control buds. Treatments with solution of pH 2.9 caused decrease of flatness of bud apical meristem during the vegetative season. Increased activity of non-specific esterase in treated buds occurred during dormancy and bud break and the enhanced accumulation of phenolic compounds was detected at the beginning of shoot growth. Changes in histochemical parameters of bud tissues were induced mainly by spraying of shoots and can thus be qualified as primary damage.     

Flowering Habit and Vegetative Behaviour in Tea (Camellia sinensis L) Seed Trees in North-East India

Apical growth of a tea shoot occurs by a succession of flushesseparated by short periods of rest. This paper describes theexternal morphology of flowering, fruiting, and abscission ofleaves of the tea plant in north-east India in relation to thephasic activity of shoot apices. All shoots on a tree make leafy growth when a new cycle of growthbegins in the spring, but terminal buds apparently become dormantas the season advances. Apparently dormant terminal buds shedbud scales, leaving on the stem a considerable number of scars,representing leafless cataphyllary flushes. These cataphyllaryflushes are produced at the same time as the leafy flushes onother shoots. A flower is formed only in the axil of a bud scale. Flowerswhich appear to develop in leaf axils are in fact inserted inthe axils of bud scales of the axillary buds. A distal leafy flush is without flowers. Flowers appear in itsleaf axils only when the terminal bud starts growth for thenext higher flush. A distal floriferous cataphyllary flush appearsas a terminal cluster of flowers. Thus, there is an acropetalsuccession of flowers, flush by flush on a caulome, determinedby the phasic activity of the apical bud. The main crop of flowers exposes anthers from the end of thethird flush (late September to early October) until the endof the winter period of growth (late January to early February).In some plants a second, minor crop of flowers appears in thespring between the end of the first and beginning of the secondflushes. In spite of considerable time lag between anthesis,the fruits produced by these two crops of flowers mature anddehisce at the same time during October to November. Abscission of leaves is also dependent upon the phasic activityof the apical buds. Only the top two flushes of a shoot possessleaves. Resumption of apical growth for a third flush, leafyor cataphyllary, causes the abscission of leaves on the lowermostof the three flushes. Two cataphyllary flushes therefore resultin the loss of all leaves on a shoot.