DEVELOPMENT AND PHYLLOTAXIS OF THE VEGETATIVE AXILLARY BUD OF MICHELIA FUSCATA

Tucker, Shirley C. (Northwestern U., Evanston, III.) Development and phyllotaxis of the vegetative axillary bud of Michelia fuscata . Amer. Jour. Bot. 50(7): 661–668. Illus. 1963.—The vegetative axillary buds of Michelia fuscala are dorsiventrally symmetrical with 2 ranks of alternately produced leaves. The direction of the ontogenetic spiral in each of these buds is related both to the symmetry of the supporting branch and to the position of the bud along the branch. On a radially symmetrical branch, all the axillary buds are alike—all clockwise, for example. But in a dorsiventrally organized branch the symmetry alternates from clockwise in 1 axillary bud to counterclockwise in the next bud along the axis. Leaf initiation and ontogeny of the axillary apical meristem conform with those of the terminal vegetative bud. The axillary bud arises as a shell zone in the second leaf axil from the terminal meristem. During this process the axillary apex develops a zonate appearance. The acropetally developing procambial supply of the axillary bud consists wholly of leaf traces. At the nodal level the bud traces diverge from the same gap as the median bundle trace of the subtending leaf. Only the basal 1–2 axillary buds which form immediately after the flowers elongate each year, while the majority remains dormant with 3 leaves or fewer.     

ONTOGENY AND PHYLLOTAXIS OF THE TERMINAL VEGETATIVE SHOOTS OF MICHELIA FUSCATA

Tucker Shirley C. (Northwestern U., Evanston, Ill.) Ontogeny and phyllotaxis of the terminal vegetative shoots of Michelia fuscata. Amer. Jour. Bot. 49(7): 722–737. Illus. 1962.—Two patterns of symmetry occur in Michelia fuscata In the lead shoots, leaves arise in a 2/5 spiral arrangement which may be either clockwise or counterclockwise. Other shoots are dorsiventrally organized; these shoots produce leaves in a modified ½ phyllotaxis in which the angle between the 2 files of leaves lies between 100° and 150°, according to the particular branch. Both types of shoot have a zonate apical meristem with a biseriate tunica a central initial zone, and a peripheral zone. The apical configuration of cells does not change appreciably during the plastochron. The flat to low-convex outline of the shoot apex is maintained by initiation of the leaves close to the summit of the apex; the diameter of the meristem diminishes greatly after such an initiation. Leaf inception in the subsurface tunica layer is followed by precocious activity of the marginal meristems which extend the stipular flanges completely around the base of the apical meristem. The stipular margins then fuse laterally and form a hood over the apex. A subapical initial meanwhile is active in the leaf blade, where it persists up to the time the leaf is 2 mm high. The most recent primordium is 300 μ high before another leaf is initiated. The vascular system of the stem is a cylindrical network of leaf traces, with 6–12 traces per leaf. The procambium develops acropetally from preexisting vascular strands in the stem below. Elements of the diverse sclereid system differ in shape in different tissues, according to the availability of intercellular space. Goebel's term “Pendelsymmetrie” is discussed with reference to apical activity in Michelia.     

ONTOGENY OF THE FLORAL APEX OF MICHELIA FUSCATA

Tucker , Shirley C. (u . Minnesota, Minneapolis.) Ontogeny of the floral apex of Michelia fuscata. Amer. Jour. Bot. 47(4): 266—277. Illus. 1960.–The floral apex of Michelia fuscata, although determinate, has a prolonged period of activity. It undergoes an increase in average height and diameter through the time of initiation of stamens, followed by a decrease in average size during initiation of successive carpels. The floral apex also shows periodic or plastochronic fluctuation in size and configuration between initiation of tiers of appendages at nearly the same level and time. Plastochrons of different duration alternate in an orderly sequence in the floral meristem.     

ORGANIZATION AND ONTOGENY OF THE VASCULAR SYSTEM IN THE PETIOLE OF EASTERN COTTONWOOD

The topologic arrangement of petiolar bundles varies within the length of the cottonwood petiole. Each petiolar bundle is formed by the subdivision and aggregation of acropetally differentiating subsidiary bundles in a predictable pattern. The subsidiary bundles provide vascular continuity between the stem and specific portions of the leaf lamina. Spot-labeling of individual veins with ¹⁴CO₂, freeze substitution, and microautoradiography were used to establish the relation between the secondary veins of the lamina and the vasculature of the petiole. Within the petiole vasculature each subsidiary bundle was continuous with a specific portion of the lamina and seemed to have a separate function. Subsidiary bundles continuous with the central leaf trace were closely related functionally to the tip region of the lamina, while the subsidiary bundles continuous with the lateral leaf traces were functionally related to the middle and basal portions of the lamina.     

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.     

DEVELOPMENT AND ORGANIZATION OF THE PRIMARY VASCULAR SYSTEM IN POPULUS DELTOIDES ACCORDING TO PHYLLOTAXY

An actively growing cottonwood bud was embedded in epon-araldite and serially sectioned at 2 μm. The sections were analyzed microscopically with the optical shuttle system of Zimmermann and Tomlinson, and all data were quantitatively recorded relative to the apex and to leaf plastochron index (LPI). Analysis of the sections revealed an acropetally developing procambial system organized according to a precise phyllotaxy. Six procambial strands could be recognized and followed long before the leaf primordia that they would enter were evident at the apex. Origin of these strands coincided with developmental events both in the parent trace and its primordium and in the antecedent leaf on the same orthostichy. Once a primordium and its trace attained a certain stage of development, trace bundles began to develop basipetally from the primordium base. These trace bundles appeared to be the earliest progenitors of wood formation in cottonwood. It was concluded that the concept of residual meristem and its corollary, the hypothesis that acropetally developing procambial strands determine the inception sties of new primordia, apply to the cottonwood apex.     

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.     

CONDUPLICATE AND SPECIALIZED CARPELS IN THE ALISMATALES

Carpel closure and stigmatic localization in the Alismatales have accompanied decreases in carpel size and numbers of ovules per carpel and increases in carpel numbers per flower. The most specialized carpels are uniovulate and indehiscent and occur acyclically in great numbers in each flower, with strong trends toward monoecism and even dioecism. The least specialized carpels in the order are open, multiovulate, and conduplicate, with poor differentiation of style and stigma. The Alismatales show a broad range from primitive to specialized gynoecial features.     

INITIATION OF STAMENS,CARPELS, AND RECEPTACLE IN THE CACTACEAE

Five taxa representing the three tribes of the Cactaceae have similar patterns of stamen and carpel initiation but display differences in early receptacle development. The first ring of stamens and the carpels arise simultaneously from subsurface layers. The bases of carpels are congenitally connate. Additional stamens are initiated centrifugally. The shape of the floral meristem within the ring created by the first stamens varies. In Pereskia corrugata it remains broadly convex; in Opuntia engelmannii it forms a depression with a small convex central region; in Epiphyllum strictum it forms a broad shallow depression; in Echinocereus reichenbachii var. albispinus it develops a deep depression; and in Mammillaria compressa it develops a depression prior to stamen and carpel initiation. Changes in receptacle shape result from cessation of apical growth and activation of an intercalary ring meristem. These two processes occur earlier in ontogeny in the more advanced of these five taxa.     

LEAF DEVELOPMENT AND PRIMARY VASCULAR ORGANIZATION IN SHOOTS OF ANISOPHYLLEA DISTICH A

Anisophyllea disticha is characterized by strong shoot dimorphism. Orthotropic shoots with helically arranged scale leaves produce tiers of plagiotropic shoots, while plagiotropic shoots are anisophyllous and bear dorsal scale and ventral foliage leaves arranged in a unique tetrastichous system. In this study we compare the patterns of leaf development and primary vascular organization in the two types of shoots. Orthotropic shoots have an open vascular system with five sympodia. Expansion of orthotropic shoot scale leaves occurs from P1 to P10–12, and leaf tissues mature precociously. Plagiotropic shoots have a closed vascular system with six sympodia. Leaves in ventral and dorsal orthostichies do not differ significantly in size until ca. P15, but ventral leaves are distinct histologically from the second node in an orthostichy, P4–6. Ventral foliage leaves have a diffuse plate meristem, and leaf expansion continues until ca. P30. Differentiation of ventral and dorsal leaf trace procambium parallels the divergent patterns of leaf expansion. These observations demonstrate the strong correlation among shoot symmetry, leaf development, and vascular differentiation within dimorphic shoots of one species.     

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 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.