AXILLARY BUD DEVELOPMENT IN POPULUS DELTOIDES. I. ORIGIN AND EARLY ONTOGENY

Origin and early development of axillary buds on the apical shoot of a young Populus deltoides plant were investigated. The ontogenetic sequence of axillary buds extended from LPI –1 (Leaf Plastochron Index) near the apical bud base to LPI –11, the fifth primordium below the bud apex. Two original bud traces diverged from the central (C) trace of the axillant leaf and developed acropetally. During their acropetal traverse the original bud traces gave rise to three pairs of scale traces. All subsequent scale traces, and later the foliar traces, were derived by divergencies from the first two pairs of scale traces. Just before the bud vascular system separated from that of the main axis, a third pair of traces diverged from the original bud traces to vascularize the adaxial scale. Concomitantly, the original bud traces were inflected toward the main vascular cylinder where they developed acropetally and eventually merged with the left lateral trace of the leaf primordium situated three nodes above the axillant leaf; they did not participate in further vascularization of the bud. During early ontogeny a shell zone formed concurrent with initiation of the original bud traces and lay interjacent to them. The shell zone defined the position of the cleavage plane that formed between the axillary bud and the main axis. The axillary bud apex first appeared in the region bounded laterally by the original bud traces and adaxially by the shell zone. Following divergence of the main prophyll traces from the original bud traces, the apex assumed a new position intermediate to the prophyll traces. Ontogenetic development suggested that the axillary bud apex may have been initiated by the acropetally developing original bud traces under the influence of stimuli arising in more mature vegetative organs below.     

DEVELOPMENT AND ORGANIZATION OF THE SECONDARY VESSEL SYSTEM IN POPULUS GRANDIDENTATA

The apical 22 cm of a dormant, first-year sprout of Populus grandidentata was sectioned serially, and the primary and secondary xylem systems were studied microscopically and graphically reconstructed. A total of 15 nodes was present on the mature stem and 14 foliar primordia in the dormant bud. The vascular traces in the lower portion of the mature stem conformed to a 2/5 phyllotaxy while those of the upper portion and within the dormant bud conformed to a 3/8 phyllotaxy. The 2/5 to 3/8 phyllotactic transition occurred in an extremely precise and systematic two-step pattern: (1) The lateral traces shifted to a new point of origin on the parent central trace, and (2) three new central traces were initiated in sequence by divergences from left-traces. Metaxylem, when followed downward, conformed to the arrangement of the procambial trace system only within one orthostichy. Below this point, the metaxylem components of lateral traces physically separated from those of the protoxylem and continued downward on a new course. Metaxylem vessels produced by the trace cambium originated from a postulated vessel-generating center at the stem-petiole junction. Each metaxylem vessel developing basipetally through the primary body was continuous with a secondary vessel developing basipetally in the secondary body. Because secondary development closed the vascular cylinder, vessels originating from developing leaves or primordia situated at higher levels in the shoot were displaced radially outward when they entered the secondary xyelm. The distribution of vessels in the secondary xylem can therefore be accounted for by a knowledge of the production and distribution of metaxylem vessels in the primary body.     

THE ORGANIZATION OF THE VASCULAR SYSTEM IN THE STEMS OF THE NYMPHAEACEAE. I. NYMPHAEA SUBGENERA CASTALIA AND HYDROCALLIS

The vascular system in the stems of Nymphaea odorata and N. mexicana subgenus Castalia, and N. blanda subgenus Hydrocallis consists of continuing axial stem bundles with eight being the usual number. The stem bundles are concentric and xylem maturation is mesarch. Xylem elements consist of tracheids with spirally or weakly reticulated secondary wall thickenings. The phloem is made up of companion cells and short sieve tube members with simple sieve plates that are nearly transverse. At the node each leaf is supplied with two lateral leaf traces and a median leaf trace. A root trace is also present and supplies a series of adventitious roots borne on the leaf base. Flowers and vegetative buds develop directly from the apical meristem and occupy leaf sites in a single genetic spiral. Each flower or vegetative bud is related to a leaf through specific spatial and vascular association. The related leaf is separated from the related flower by three members of the genetic spiral and occupies an adjacent orthostichy. Vascular tissue for the related flower arises from the inner surfaces of the four stem bundles supplying leaf traces to the related leaf and extends through the pith to the flower or vegetative bud via a peduncle fusion bundle. The vascular system organization in the investigated species of Castalia and Hydrocallis is not typically monocotyledonous or dicotyledonous, nor can it be considered transitional between them. The ontogeny of the vascular system is similar to typical dicotyledons and the investigated species of Nymphaea can, therefore, be considered to represent highly specialized and modified dicotyledons.     

ESTABLISHMENT OF THE VASCULAR SYSTEM IN SEEDLINGS OF POPULUS DELTOIDES BARTR.

Seven seedlings ranging from 1 to 25 days old were embedded in Spurr's resin and serially sectioned at 1–2 μm. Sectioning extended from well above the apex downward to the hypocotyl base in the 1–day seedlings and to varying levels in the hypocotyl in the older seedlings. Procambial development was analyzed in its entirety for each seedling, and a composite two-dimensional diagram representing the procambial system of a 25-day-old seedling was prepared. Each cotyledon was served by a double-trace, one-half of which was derived from each of two embryonic bundles. The central traces serving the four primary leaves were in turn derived from the four cotyledonary bundles comprising the double traces. The procambial system serving the cotyledons and the four primary leaves approximated a decussate phyllotaxy. The central traces serving the secondary leaves were arranged in a helix that conformed at first to a 1/3 and then to a 2/5 phyllotaxy. Transitions to higher phyllotactic orders were systematic and reproducible, and they occurred in an orderly sequence in both the central and lateral leaf traces. The manner in which leaf traces diverged from parent traces to serve new leaf primordia provided for vascular redundancy. Thus, the entire vascular system was integrated into a highly functional whole.     

Ontogeny of the proventitious epicormic buds in Quercus petraea.

In the present work, we described the fate of proventitious epicormic buds on the trunks of 40-year-old Quercus petraea trees and in parallel the vascular trace they produced in the wood. Our results show that small and large individual epicormic buds can survive as buds for 40 years and that both are composed of a terminal meristem and scales. Meristematic areas are detected in the scale axils of small buds; in addition to these meristems the large buds also have secondary bud primordia. The small buds are connected to the pith of the main stem by a unique trace, whereas the large buds are connected by one or multiple traces. A single trace might imply that the whole bud is still alive and multiple traces might indicate that the terminal meristem has died. In the latter case, each trace is connected to a secondary bud of the large bud. The buds found in a cluster are composed of a terminal meristem and scales with axillary meristems in the scale axils. A cluster is connected to the pith of a stem either by a unique trace when it seems to be the result of partial abscission of an epicormic shoot or multiple traces when it might have originated from an epicormic bud in which the terminal meristem has died. Whatever the type of the bud, the vascular trace in the bark is composed of a cambium, secondary xylem and parenchyma cells and the trace present in the wood had parenchyma cells with vestiges of secondary xylem. Each year, the vascular trace should be produced in the bark by the cambium of the tree but not by the bud itself. On 40-year-old Q. petraea, we observed a proliferation of epicormic buds and in parallel a multiplication of the number of vascular traces in the trunk, but the knots caused by the traces of epicormic buds in the wood, either as individuals or in clusters, are minor since their colours are only slightly darker than those of woody rays and they are less than 2 mm in diameter. The knots will appear when epicormic buds develop into shoots. Received: 30 March 1999 / Accepted: 09 June 1999     

THE ORGANIZATION OF THE VASCULAR SYSTEM IN THE STEMS OF THE NYMPHAEACEAE. II. NYMPHAEA SUBGENERA ANECPHYA,LOTOS, AND BRACHYCERAS

The anatomy and organization of the stem vascular system was analyzed in representative taxa of Nymphaea (subgenera Anecphya, Lotos, and Brachyceras). The stem vascular system consists of a series of concentric axial stem bundles from which traces to lateral organs depart. At the node each leaf is supplied with a median and two lateral leaf traces. At the same level a root trace supplies vascular tissue to adventitious roots borne on the leaf base. Flowers and vegetative buds occupy leaf sites in the genetic spiral and in the parastichies seen on the stem exterior. Certain leaves have flowers related to them spatially and by vascular association. Flowers (and similarly vegetative buds) are vascularized by a peduncle trace that arises from a peduncle fusion bundle located in the pith. The peduncle fusion bundle is formed by the fusion of vascular tissue derived from axial stem bundles that supply traces to certain leaves. The organization of the vascular system in the investigated taxa of Nymphaea is unique to angiosperms but similar to other subgenera of Nymphaea.     

Vascular inter-relationships in someSolanaceae members

Vascular inter-relationships between axillary bud, axillant leaf and axis have been studied in fives pecies of theSolanaceae, Lycopersion lycopersicum (L. )Karsten,Cestrum nocturnum L.,Cestrum diurnum L.,Withania somnifera (L.)Dunal, andDatura innoxia Mill. The phyllotaxy is alternate and the node is unilacunar with one or more leaf trace strands. The bud traces arise either from the trace of the subtending leaf or of the strands flanking the leaf gap. The vascular relationship between the bud, axillant leaf and main axis is discussed.     

SHOOT VASCULAR SYSTEM AND PHYLLOTAXIS OF CASUARINA (CASUARINACEAE)

In species of Casuarina with multileaved whorls, each stem vascular bundle divides radially into two at the site of a leaf trace separation, and the same two bundles rejoin acropetally to where the trace supplies a leaf. Such divisions are divisions of a single vascular bundle, and the rejoining of bundles forms a single bundle. Proposals that the extant primary vascular systems of dicotyledons may have been derived as in conifers are incorrect in so far as Casuarina is concerned, or the system has evolved beyond that so far proposed for dicotyledons. Reasons are offered, however, for considering that fernlike leaf gaps are not present. Leaf traces supply leaves at the first nodes distal to their origins. The ways by which an increase or decrease of stem bundles occur are described. Phyllotactic patterns range from helical (rare) to whorled. In the embryo, where leaves occur decussately, of certain species with multileaved whorls, and in the shoot apices of species with tetramerous whorls, slight differences in the levels of leaf attachments and the bending of leaf traces indicate the probable evolution of extant whorled phyllotaxies from one or more helical arrangements. Stages in the evolution are suggested. The leaves in most species with multileaved whorls are in true whorls. The original periderm of branchlets lies internally to the internodal traces and chlorenchyma, but is otherwise external to the vascular system. It is concluded that each leaf originates at its level of separation from the axis despite several structural features suggesting that the leaf bases have become congenitally adnate to the stem.     

THE ORGANIZATION OF THE VASCULAR SYSTEM IN THE STEMS OF THE NYMPHAEACEAE. III. VICTORIA AND EURYALE

Organization of the stem vascular system was analyzed in Victoria species and Euryale ferox. The stem vascular system consists of a number of concentrically-organized continuing axial stem bundles. At the node each leaf is supplied with a root trace, two lateral leaf traces, and a median leaf trace. A peduncle fusion bundle is also present at each node. The peduncle fusion bundle supplies vascular tissue to the median leaf trace and to the peduncle trace. Flowers are nonmedian axillary but have specific vascular, spatial, and developmental relationships to leaves in a manner that resembles the genus Nymphaea. On the basis of the analysis of the stem vascular system, Victoria and Euryale are more similar to each other than to Nymphaea. However, the vascular system in Victoria and Euryale is similar enough to Nymphaea to suggest that Nymphaea, Victoria, and Euryale form a natural taxon of unique angiosperms. The organization of the stem vascular system in Victoria and Euryale is dicotyledonous.     

MORPHOLOGICAL STUDIES OF THE NYMPHAEACEAE (SENSU LATO). XIII. CONTRIBUTIONS TO THE VEGETATIVE AND FLORAL STRUCTURE OF CABOMBA

Six species of Cabomba have been examined although the anatomy of the vegetative axes is based on the study of only C. caroliniana and C. palaeformis. A plant consists of an erect short shoot with decussate leaves which bears axillary flowering shoots and rhizomes. A rhizome bears decussate leaves and may also form axillary flowering shoots or turn upward and become a new short shoot. The phyllotaxies of the flowering shoots are proximately decussate or ternate (C. piauhyensis). The flowering shoots with decussate phyllotaxy change to 1/3 phyllotaxy distally; they bear axillary flowers proximally, and extra-axillary flowers distally. Flowering shoots with ternate phyllotaxy do not change distally but each produces first axillary and then extra-axillary flowers. Decussate vegetative axes and flowering shoots have four vascular bundles; ternate vegetative axes and flowering shoots have six vascular bundles, distantly paired into two or three vascular bundle-pairs, respectively. An elliptical vascular plexus occurs at each node. Each leaf receives one bundle-pair from one trace and each flower three bundle-pairs. A two-level receptacular vascular plexus occurs in flowers; the proximal, larger portion provides traces to perianth and stamens and the distal, smaller portion becomes carpellary traces. Each of the three sepals typically receives five branch traces from a basal principal trace, and each of the three petals receives, typically, three branch traces from a basal principal trace. Sepals and petals generally occur in a single, basally connate whorl. Each stamen receives one trace. Each stamen of three-stamen flowers is opposite a petal; each stamen of six-stamen flowers is aligned with an interval between a petal and adjacent sepal. Each staminal trace, which is just above the principal petal trace, in a three-petal flower, is frequently adnate to the latter trace. Each carpel receives one principal trace from the distal, small extension of the receptacular plexus, and each principal trace becomes three conventional veins of a carpel. Ovules may be borne directly over one of the veins or in any position between veins and are supplied by branches of the nearest vein or nearest two veins. All traces, ovular supply veins and the proximal portions of all veins are amphicribral. The several anatomical and morphological differences in vegetative axes and flowers between Cabomba and Brasenia suggest a greater taxonomic distance between the two genera than commonly supposed. It is suggested that extra-axillary flowers in 1/3 helical and ternate flowering shoots of Cabomba might be advantageous in preventing anthesis of flowers beneath peltate leaves. The aberrant position might be the initial evolutionary step toward what, in other nymphaeaceous genera, has shifted each flower to an adjacent helix. It is proposed that the zigzag stem accompanying the trigonal and sympodial flowering shoots may offer greater stability and floatability in water than the monopodial form. Several suggestions are offered for the variability of ovular positions: 1) the variability is a vestige of former laminar placentation in conduplicate carpels; 2) it is a vestige of a primitive condition antedating the current close association of ovules with ventral carpellary veins; 3) it is an early stage of evolution which might have terminated in laminar placentation and cantharophily, but which was replaced by a trend toward myophily.     

VASCULARIZATION OF A MULTILACUNAR SPECIES: POLYSCIAS QUILFOYLEI (ARALIACEAE) I. THE STEM

The odd-pinnate leaves of Polyscias quilfoylei have a sheathing leaf base that completely encircles the stem. At each node, many traces depart the vascular cylinder and traverse an obliquely upward course through the leaf base before aggregating in the rachis. Lateral traces diverge from parent traces in the stem vasculature at variable times relative to the leaf they serve, from variable positions in the vascular cylinder and from parent traces of variable ages. The stem vasculature is formed by the coalescing of leaf traces from as many as five leaves. All bundles departing the vascular cylinder at a node to serve a leaf are true leaf traces originating independently in the stem. Leaf traces develop acropetally from their positions of origin on parent traces. Primordial leaves are first served by the median trace and later by lateral traces. Many traces were recognized in the internodes subtending embryonic leaves, but they could not be related either to a specific leaf or to a specific position within a leaf. Because these traces had not yet achieved contact with a primordial leaf site, they were assumed to be in the process of developing acropetally at the time of sampling. Observations suggest that the multiple traces in this species might perform a similar function of integrating the vascular cylinder that subsidiary bundles perform in certain uni- and trilacunar species.     

VASCULAR ORGANIZATION IN SHOOTS OF CACTACEAE. I. DEVELOPMENT AND MORPHOLOGY OF PRIMARY VASCULATURE IN PERESKIOIDEAE AND OPUNTIOIDEAE

Primary shoot vasculature has been studied for 31 species of Pereskioideae and Opuntioideae from serial transections and stained, decorticated shoot tips. The eustele of all species is interpreted as consisting of sympodia, one for each orthostichy. A sympodium is composed of a vertically continuous axial bundle from which arise leaf- and areole-trace bundles and, in many species, accessory bundles and bridges between axial bundles. Provascular strands for leaf traces and axial bundles are initiated acropetally and continuously within the residual meristem, but differentiation of procambium for areole traces and bridges is delayed until primordia form on axillary buds. The differentiation patterns of primary phloem and xylem are those typically found in other dicotyledons. In all species vascular supply for a leaf is principally derived from only one procambial bundle that arises from axial bundles, whereas traces from two axial bundles supply the axillary bud. Two structural patterns of primary vasculature are found in the species examined. In four species of Pereskia that possess the least specialized wood in the stem, primary vascular systems are open, and leaf traces are mostly multipartite, arising from one axial bundle. In other Pereskioideae and Opuntioideae the vascular systems are closed through a bridge at each node that arises near the base of each leaf, and leaf traces are generally bipartite or single. Vascular systems in Pereskiopsis are relatively simple as compared to the complex vasculature of Opuntia, in which a vascular network is formed at each node by fusion of two sympodia and a leaf trace with areole traces and numerous accessory bundles. Variations in nodal structure correlate well with differences in external shoot morphology. Previous reports that cacti have typical 2-trace, unilacunar nodal structure are probably incorrect. Pereskioideae and Opuntioideae have no additional medullary or cortical systems.     

XYLARY UNION BETWEEN THE NEW SHOOT AND OLD STEM DURING TERMINAL BUD BREAK IN POPULUS DELTOIDES

Bursting terminal buds and subtending stems of Populus deltoides Bartr. ex Marsh. plants were examined at several stages to determine the pattern of xylary union between the 1st- and 2nd-yr growth increments. Metaxylem vessels differentiated first in traces serving the basalmost leaf in the bud. As successively younger leaves began growth, metaxylem vessels differentiated in their traces. The site of metaxylem reactivation was in the second or third internode beneath the bud (i.e., in the 1st-yr stem), and subsequent differentiation progressed bidirectionally in each set of traces as the leaves they served expanded. Traces leading either to abscised leaf positions on the 1st-yr stem or to bud-scale leaf positions were reactivated by the tangential “spread” of activity from adjacent traces serving expanding leaves. The new elements were all secondary xylem vessels, as were those of the basipetal trace components, although they were functionally continuous with the metaxylem vessels that differentiated acropetally. Xylem fibers were initiated in the same position and differentiated in the same sequence as vessels. However, fiber differentiation lagged behind that of vessels. Whereas vessel differentiation was associated with leaf expansion, fiber differentiation was associated with leaf maturation. As each leaf matured in sequence, the primary-secondary transition zone advanced acropetally to the bud base and then in the new shoot until it attained a positional relation with leaf maturation comparable to that of 1st-yr plants.     

Ontogeny of the vascular system ofBotrychium multifidum (S. G. Gmelin) Rupr.(Ophioglossaceae) and its bearing on stellar theories

Basipetal to the shoot apex, a procambial ring with parenchymatous gaps is present. The protoxylem poles are endarrh in both the ectophloic siphonostele and the collateral vascular bundle which comprises the leaf trace. Each leaf trace has an anastomosing system of protoxylem poles that decreases in number basipetally from five to three to two. Differentiation of the leaf trace procambium and protoxylem is bidirectional, that is the differentiation first occurs near the base of the leaf and acropetally in the leaf and basipetally in the stem. Then a fascicular cambium differentiates betweem the primary xylem and phloem in the leaf. This vascular cambium which is also present in the stem is unidirectional and only produces secondary xylem centripetally. Limited secondary growth also occurs in roots. Medullary tracheids when present are longitudinally continuous with the vascular system. The stele of the stem is interpretated as a sympodium of leaf traces and the pith is considered to be fundamental tissue enclosed by the anastomosing of leaf traces.     

INITIAL VASCULARIZATION OF THE VEGETATIVE SHOOT OF ABIES CONCOLOR

Parke , Robert V. (Colorado State U., Fort Collins.) Initial vascularization of the vegetative shoot, of Abies concolor. Amer. Jour. Bot. 50(5): 464–469. Illus. 1963.—In the dormant winter bud, the future vascular system of the shoot exists as a rather ill-defined system of procambial strands, which extends acropetally from the scale traces through a plate of thick-walled, deeply staining cells, the crown, and into the axis and the numerous foliar primordia making up the telescoped shoot. Each foliar primordium receives a single procambial strand or leaf trace. The procambial strands differentiate acropetally. No differentiated vascular tissue was observed in the dormant shoot. As the shoot elongates in the spring, vascular differentiation progresses at a rapid rate. In the leaf traces, protophloem differentiates acropetally. The protoxylem, which appears first in the axial region of the trace, differentiates acropetally into the foliar primordium and basipetally into the stem. The first-formed phloem elements are short-lived. They are nucleate and without sieve areas. In the protoxylem, the first-formed tracheids are mostly of the annular or spiral-thickened type.     

VASCULARIZATION OF DEVELOPING LEAVES OF GLEDITSIA TRIACANTHOS L. I. THE NODE,RACHIS, AND RACHILLAE

Leaves of Gleditsia triacanthos L. are served by three leaf traces that subdivide in the node to produce subsidiary bundles. The subsidiary bundles differentiate basipetally in the stem and acropetally in the petiole using the original leaf trace bundles (those that developed acropetally) as templates for their development. Within the pulvinus, the acropetal bundle components merge to form the rachis vasculature consisting of a semicircular arc and a ventral chord; several small bundles diverge to form ventral ridge bundles. Mixing of bundles occurs during vascularization of the lateral rachillae axes. Each diverging rachilla axis receives bundles from the semicircular arc, the ventral chord, and a ridge bundle in a relatively reproducible and predictable pattern. During this process the main rachis vasculature is gradually depleted, but the ridge bundles are reconstituted following divergence of each rachilla pair. The distal rachilla pair is vascularized by a bilateral partitioning of the entire rachis vasculature; a remnant of the central leaf trace terminates in a subulate terminal appendage. Vascularization of the bipinnate G. triacanthos leaf is compared to that of the simple Populus deltoides leaf.     

The Vascular Pattern of Italian Ryegrass (Lolium multiflorum Lam.) 4. The Peripheral Plexus, and Nodal Root Insertion

The interconnecting system of leaf traces constitutes only afraction of the vascular tissue found in the base of a ryegrassstem. The tillers and nodal roots have their insertion in thiscongested region of the plant in addition to the majority ofthe leaf traces. Study of the attachment of nodal roots revealsthe extensive differentiation of vascular tissue in a perforatedcylinder surrounding the inner leaf trace system—the peripheralplexus. This plexus consists of two components, the diffuse bundlesorientated along the stem axis, and interconnected with theroot girdles orientated around the stem axis. The peripheralplexus which is bounded externally by a mestome sheath, makesnumerous contacts with the leaf trace system within it, bothdirectly and via the nodal plexi, and receives the vascularattachment of all the nodal roots. It appears in the stem atabout the same time as adjacent nodal roots, and differentiatesfrom meristematic tissue totally independently of the leaf tracesystem. The diffuse bundles themselves apparently differentiateacropetally in this meristematic tissue and are augmented bybranches from leaf traces and the nodal plexi. The integrated vascular systems of leaf, stem, and root at thebase of the grass plant, bounded by a mestome sheath, must allowtotal intercommunication between all organs. Nearly all tissuewithin the mestome sheath is vascular in nature and it is intothis vascular tissue that the leaf traces associated with transfercells are inserted.     

Ontogeny and histochemistry of axillary bud inMurraya koenigii L. spreng

Histochemical localization of total proteins, histories, nucleic acids, ascorbic acid and polysaccharides in the developing axillary bud ofMurraya koenigii and its vascular relationship with the main axis are investigated. All the above variable metabolites are richly distributed throughout the bud development. The shell zone is indicative of poor distribution of these metabolites. Histochemical tests prove that the axillary bud is metabolically very active. The initiation of the axillary bud is in the axil of the 2nd leaf where two cells of 2nd tunica layer become prominent and undergo periclinal divisions to give rise to the bud. The bud maintains tunica-corpus organization throughout its development. The cells of the shell zone at the base of the bud differentiate into pith meristem of the bud. The axillary bud has two bud traces which are associated with vascular strands that are not the traces of the subtending leaf.     

VASCULAR CONSTRUCTION AND DEVELOPMENT IN THE AERIAL STEM OF PRIONIUM (JUNCACEAE)

The aerial stem of Prionium has been studied by motion-picture analysis which permits the reliable tracing of one among hundreds of vascular strands throughout long series of transverse sections. By plotting the path of many bundles in the mature stem, a quantitative, 3-dimensional analysis of their distribution has been made, and by repeating this in the apical region an understanding of vascular development has been achieved. In the mature stem axial continuity is maintained by a vertical bundle which branches from each leaf trace just before this enters the leaf base. Lateral continuity results from bridges which link leaf traces with nearby vertical bundles. Development of the provascular system involves a meristematic cap into which the blind ends of vertical bundles can be followed. Leaf traces are produced continuously in association with developing leaf primordia for a period of over 30 plastochrones; they connect with the vertical bundles in the meristematic cap and so establish the essential vascular configuration which is later reorientated through about 90° by overall growth of the crown. The last bundles to differentiate from the leaf do so outside the meristematic cap and thus fail to make contact with the axial system; they appear in the mature axis as blind-ending cortical bundles. Prionium is only distantly related to palms and its vascular histology is quite different. Nevertheless, the course of vascular bundles and the origin of this pattern in the stem resembles that of a palm. It is suggested that we are examining the fundamental pattern of vascular development in large monocotyledons.     

PROCAMBIUM VS. CAMBIUM AND PROTOXYLEM VS. METAXYLEM IN POPULUS DELTOIDES SEEDLINGS

The concept of a procambium-cambium continuum was examined in Populus deltoides by following its development in serially sectioned bud and stem tissues. As in other species, the term cambium is used to refer to that part of the continuum associated with the formation of secondary vascular tissues; i.e., with secondary growth. However, that part of the continuum associated with the formation of primary vascular tissues is subdivided to facilitate interpretation of the consecutive stages of primary xylem differentiation. Thus, the procambium as envisioned by other authors is subdivided into procambium, initiating layer, and metacambium, all of which develop acropetally and in complete continuity. The procambium is derived from the residual meristem in the form of acropetally developing strands and traces. The initiating layer is represented by the first, tangentially separated, periclinal divisions that delineate the position of the prospective cambium. The metacambium is a later stage during which additional periclinally dividing cells unite the initiating layer into a tangentially continuous meristem within a trace bundle. After establishment of the initiating layer, the procambial trace is completely phloem dominated. Protoxylem differentiation begins in an originating center at the base of the leaf primordium and it progresses basipetally to form the protoxylem pole. Cells of the initiating layer do not contribute to the formation of either protoxylem or protophloem. However, those cells of the initiating layer directly opposite the protoxylem pole divide precociously and later differentiate to metaxylem, thus forming a radial file of protoxylem-metaxylem elements. Protoxylem elements of lateral traces are longitudinally continuous with the protoxylem of their parent traces, whereas those of a central trace are longitudinally continuous with the metaxylem of its parent trace. Metaxylem is formed later than protoxylem and it is derived from the metacambium. Metaxylem does not form a continuous system with protoxylem of the same trace because of the different temporal and spatial origins of the two kinds of xylem. Rather, metaxylem is longitudinally continuous with secondary xylem of older traces below. An attempt was made to determine the functional significance of the pattern of protoxylem and metaxylem differentiation in relation to primary and secondary plant development.