THE VASCULAR SYSTEM OF THE INFLORESCENCE AXIS OF ANDROPOGON GERARDII (GRAMINEAE) AND ITS BEARING ON CONCEPTS OF MONOCOTYLEDON VASCULAR TISSUE

The vascular bundles in the inflorescence axis of Andropogon gerardii occur in inner and outer systems. The inner system is made up of large, early developing strands that, at earliest stages of development, are precocious (= the appendage they are to serve has not yet been initiated). The outer system consists of later developing smaller strands that are open ended in a proximal direction (= strands differentiate basipetally in the cortex below the appendage they serve). Bundles of both the inner and outer systems are not connected to other procambium early in their development but exist as isolated strands. The veins of the inner system of the inflorescence axis occur as sympodia. The presence of inner and outer systems in the vascular tissue is common to most monocotyledons. However, amongst monocotyledons, only certain grasses have been shown to have strands of the inner system that are isolated early in development. Many dicotyledons have large strands which are precocious and some have smaller, later developing strands which are open ended in a proximal direction, hence they occur as isolated strands. These smaller strands in dicotyledons occur between large strands. Certain dicotyledons have an inner and an outer system of veins. Of these, some have veins of the inner system that differ from the inner system bundles of monocotyledons in that they also form part of the outer system of veins, or develop at a different time. One other dicotyledon with an inner and outer system, Bougainvillea, differs from monocotyledons only in that the bundles of the outer system do not seem to be isolated early in their development and anastomoses are seen between the inner and outer systems. Thus, it appears that monocotyledons differ from dicotyledons only in the presence of independent inner and outer systems of vascular bundles in the former. Thus, the hypothesis of Zimmermann and Tomlinson that there are basic differences between monocotyledon and dicotyledon vascular systems is not substantiated. It is even suspected that monocotyledon and dicotyledon vascular systems will be demonstrated to be modifications of a basic plan consisting of large, acropetally differentiating and smaller, basipetally differentiating strands.     

RE-EVALUATION OF CERTAIN KEY RELATIONSHIPS IN THE ALISMATIDAE: FLORAL ORGANOGENESIS OF SCHEUCHZERIA PALUSTRIS (SCHEUCHZERIACEAE)

Transition to flowering in the North-temperate bog plant Scheuchzeria palustris occurs in early May and results in the formation of a simple raceme with six flowers. Five of the flowers are subtended by large foliar bracts, while the sixth and last-formed flower on the inflorescence remains ebracteate. The individual flowers develop along a clearly trimerous pattern. The three outer tepals develop first, arising almost simultaneously at the periphery of the triangular floral apex. They are followed closely by the development of the three anti-tepalous outer stamens. The three inner tepals are next in the developmental sequence, alternating with the outer whorl of tepal-stamen pairs but arising at a slightly higher level on the floral meristem. Three inner stamens are initiated opposite the inner tepal primordia. Finally, three gynoecial primordia are initiated on the remaining central portion of the floral apex and alternating with the inner whorl of tepal-stamen pairs. Each carpel develops at first as a horseshoe-shaped structure. Two ovules form in each carpel, initiating on the adaxial margin of the carpel wall. Histogenesis of all floral appendages involves initially periclinal divisions in the second tunica layer followed by corresponding anticlinal divisions in the first tunica layer and concurrent activity in the underlying corpus. Separate procambial strands differentiate acropetally from the inflorescence axis to each tepal-stamen pair and then bifurcate. The vascular connection to the gynoecium develops directly from the strands in the tepal-stamen pairs. The results of this developmental study of the flower of S. palustris have a significant bearing on the positioning of this and related taxa within the Alismatidae and on the speculation of the phylogeny of the monocotyledon flower.     

ONTOGENY OF THE PRIMARY THICKENING MERISTEM IN SEEDLINGS OF BOUGAINVILLEA SPECTABILIS

Anomalous secondary thickening occurs in the main axis of Bougainvillea spectabilis as a result of a primary thickening meristem which differentiates in pericycle. The primary thickening meristem first appears in the base of the primary root about 6 days after germination and differentiates acropetally as the root elongates. It begins differentiating from the base of the hypocotyl toward the shoot apex about 33 days after germination. The primary thickening meristem is first observable at the base of the first internode about 60 days after germination. It then becomes a cylinder in the main axis of the seedling. No stelar cambial cylinder forms in the primary root, hypocotyl, or stem because vascular cambium differentiation occurs neither in the pericycle opposite xylem points in the primary root nor in interfascicular parenchyma in the hypocotyl or stem. The primary vascular system of the stem appears anomalous because an inner and an outer ring of vascular bundles differentiate in the stele. Bundles of the inner ring anastomose in internodes, whereas those of the outer ring do not. Desmogen strands each of which is composed of phloem, xylem with both tracheids and vessels, and a desmogic cambium, differentiate from prodesmogen strands in conjunctive tissue. The parenchymatous cells surrounding desmogen strands then differentiate into elongated simple-pitted fibers and thick-walled fusiform cells that are about the same length as the primary thickening meristem initials.     

DEVELOPMENTAL STUDIES IN PTYCHOSPERMA (PALMAE). I. THE INFLORESCENCE AND THE FLOWER CLUSTER

This paper describes inflorescence structure, including organogenesis of the panicle and flower clusters and vasculature of flowering branches, for two species of Ptychosperma, a genus of arecoid palms. The inflorescence is an infrafoliar panicle with up to four orders of branches in a spirodistichous arrangement conforming to an irregular one-half phyllotaxy. The primordium of the inflorescence is crescentic and the apex has two tunica layers, a group of central cells, and a rib meristem. The distal flower-bearing parts or rachillae of all branches develop acropetally early in ontogeny and are vertically oriented in the bud. Although these rachillae terminate branches of different sizes and orders, they are similar in size and in number of flower clusters produced. Internodes and lower parts of branches develop later. Bracts of four types are produced: a prophyll and empty peduncular bract, bracts which subtend lateral branches, bracts subtending triads, and floral bracteoles. The prophyll and peduncular bracts are tubular and completely closed around all branches until about three months before the flowers reach anthesis. Bracts subtending lateral branches and those that subtend triads enlarge by small amounts of apical, adaxial, and marginal growth to cover subtended apices during early ontogeny, but are small to absent at maturity. Flower clusters are triads of two lateral staminate and a central pistillate flower. Organogenesis indicates that the triad is a sympodial unit. Flowers develop successively, each floral apex bearing a bracteole that subtends the next flower. The vasculature of the inflorescence may be divided into two systems. Bundles of the main axis extend acropetally into the vertically oriented branches as they are initiated and form a central cylinder of larger bundles in each branch. Flower clusters are supplied by a peripheral system of smaller bundles that develop later in relation to the developing floral organs. Bundles of the peripheral system branch frequently, but branching levels are irregular. The irregular branching of peripheral bundles appears related to the phyllotaxy of the flower clusters and the random right or left position of the first flower of the triad. The level of branching of a bundle may depend on the position of a floral primordium with respect to an existing procambial strand. Three (-4) bundles supply each staminate flower and six (-10) the pistillate flower. The histologically specialized inflorescence has stomata and contains abundant starch. Tannins and raphides, spherical silica bodies, and various forms of sclerenchyma appear in sequence and apparently provide support and protection during the long exposure of the branches.     

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.     

AXILLARY AND DICHOTOMOUS BRANCHING IN THE PALM CHAMAEDOREA

In both Chamaedorea seifrizii Burret and C. cataractarum Martius each adult foliage leaf subtends one axillary bud. The proximal buds in C. seifrizii are always vegetative, producing branches (= new shoots or suckers); and the distal buds on a shoot are always reproductive, producing inflorescences. The prophyll and first few scale leaves of a vegetative branch lack buds. Transitional leaves subtend vegetative buds and adult leaves subtend reproductive buds. Both types of buds are first initiated in the axil of the second or third leaf primordia from the apex, P2 or P3. Later development of both types of bud tends to be more on the adaxial surface of the subtending leaf base than on the shoot axis. Axillary buds of C. cataractarum are similarly initiated in the axil of P2 or P3 and also have an insertion that is more foliar than cauline. However, all buds develop as inflorescences. Vegetative branches arise irregularly by a division of the apex within an enclosing leaf (= P1). A typical inflorescence bud is initiated in the axil of the enclosing leaf when it is in the position of P2 and when each new branch has initiated its own P1. No scale leaves are produced by either branch and the morphological relationship among branches and the enclosing leaf varies. Often the branches are unequal and the enclosing leaf is fasciated. The vegetative branching in C. cataractarum is considered to be developmentally a true dichotomy and is compared with other examples of dichotomous (= terminal) branching in the Angiospermae.     

STUDIES ON THE ONTOGENY OF THE DWARF MISTLETOES,ARCEUTHOBIUM. III. DEVELOPMENT OF THE INFLORESCENCE

In vascular plants, the apical meristem of the shoot normally represents a continuation of growth in the apical meristem of the embryo itself. This is not the case in Arceuthobium. Here the shoot apex of the embryo is rudimentary and eventually dies after infection of the host occurs. The inflorescence of Arceuthobium is, therefore, an adventitious structure originating in the endophytic system rather than from the shoot apex of the seedling. Inflorescence buds arise in either of 2 ways. In some species (A. douglasii and A. americanum), buds first appear as small meristematic protuberances on the outer surface of cortical strands. In other species (A. campylopodum), the buds arise at the ends of short branches. The former, or diffuse, type gives rise to inflorescences along the entire surface of the host branch; in the latter, or condensed, type inflorescences are formed in clusters. Early ontogeny of the inflorescence apex of both types is described. Studies of subsequent growth of the inflorescence apex show 5 well-defined plastochronic stages: (1) maximal area stage; (2) minimal area stage; (3) early post-minimal stage; (4) late post-minimal stage; and (5) pre-maximal stage.     

DEVELOPMENT OF THE EPIPHYLLOUS INFLORESCENCE OF HELWINGIA JAPONICA (HELWINGIACEAE)

The inflorescence of Helwingia japonica (Thunb.) Dietr. is initiated adjacent to the leaf axil on the adaxial side of the base of a leaf primordium during its second plastochron. The inflorescence which develops from the resulting primordium comes to be situated on the midrib of the mature fertile leaf, through the action of a basal, intercalary meristem. In fertile leaves this meristem develops beneath, as well as above, the insertion of the inflorescence primordium on the leaf primordium. The same meristem is present in sterile leaves as well. A separate, adaxial vascular bundle departs from the leaf trace in the base of the petiole and leads to the inflorescence, in the mature fertile leaf. This adaxial vascular bundle is absent in sterile leaves. It is argued that the vascular anatomy does not conclusively confirm the hypothesis that the epiphyllous inflorescence is the congenital fusion product of a leaf and an axillary inflorescence. Instead, it is suggested that the interplay of changes in the position of primordium initiation, and intercalary growth, offers an ontogenetic explanation of the situation, which in turn may be related to the phylogeny of the species in question. It appears to be misguided and futile to look for homologies (i.e., 1:1 correspondences) between fertile and sterile leaves, since 1:1 correspondences do not exist in this case.     

PHYLLODE THEORY IN RELATION TO LEAF ONTOGENY IN SANSEVIERIA TRIFASCIATA

Shoot apices of Sansevieria trifasciata have a three-layered mantle, a zone of subapical initials, a central meristem, and a peripheral meristem. Leaf initiation begins with periclinal divisions in L-3 and is followed by periclinal divisions in L-2 and anticlinal divisions in L-l. At first, the primordium is a mound of tissue at one point on the flank, but it soon takes the form of a low ridge encircling the apex. An ephemeral adaxial meristem differentiates in L-2 of the primordium when it is about 50 μ high and is active until the primordium is about 450 μ high. Then it ceases basipetally and is not observable after the primordium is about 600μ high. As the adaxial meristem ceases at the base of the radial tip, its two lateral regions become the submarginal meristems of the expanded portion. Marginal meristems differentiate from the protoderm, and oblique-anticlinal divisions of the marginal initials result in the formation of an abaxial and adaxial epidermis. These derivatives undergo a few anticlinal divisions, increasing marginal width, and then they divide periclinally, increasing marginal thickness. After the primordium is about 600-700 μ high it continues to grow in length by a diffuse basal intercalary meristem. When the leaf is 3 dm long, an adaxial rounding meristem differentiates in the region just above the sheath. Leaf vasculature consists of parallel bundles which anastomose acropetally. Vascular bundles are arranged in a semicircle in the expanded portion and in a circle in the radial tip. There is one centrally located bundle at the apex as a result of lateral anastomoses. Present evidence from leaf ontogeny and mature vasculature in S. trifasciata is interpreted as supporting the concept that the liliaceous leaf is homologous with the phyllodes of A corns and Acacia.     

Leaf and inflorescence peduncle anatomy: a contribution to the taxonomy of Rapateaceae

The anatomy of leaves and inflorescence peduncles was studied in species of Monotrema (4), Stegolepis (1) and Saxofridericia (1), aiming to contribute to the taxonomy of Rapateaceae. The form and structure of leaf blade midrib and the form of the inflorescence peduncle are diagnostic characteristics for the studied species. Monotrema is distinguished by: epidermal and vascular bundle outer sheath cells containing phenolic compounds in both organs; leaf blade with palisade and spongy chlorenchyma, arm-parenchyma, and air canals between the vascular bundles; leaf sheath with phenolic idioblasts in the mesophyll; inflorescence peduncle with tabular epidermal cells and air canals in the cortex and pith. Such characteristics support the recognition of Monotremoideae, which includes Monotrema. Stegolepis guianensis is distinguished by thick-walled epidermal cells and a plicate chlorenchyma in both organs; leaf blade with subepidermal fiber strands in abaxial surface and a heterogeneous mesophyll; inflorescence peduncle with rounded epidermal cells, a hypodermis with slightly thick-walled cells, and a pith with isodiametric cells and vascular bundles. Saxofridericia aculeata is distinguished by papillate epidermal cells in both organs; unifacial leaf blade with subepidermal fiber strands in both surfaces and a regular chlorenchyma; leaf sheath with a hypodermis in both surfaces and fiber bundles in the mesophyll; inflorescence peduncle with an undefined cortex and a hypodermis with thick-walled cells. S. guianensis shares few characteristics with S. aculeata, supporting their placement in different tribes.     

DIFFERENTIATION AND CONTINUITY OF THE PHLOEM IN THE LEAF INTERCALARY MERISTEM OF LOLIUM PERENNE

Serial transverse sections of the stem tip and leaf bases of immature perennial ryegrass leaves were examined to assess the effect of the intercalary meristem on assimilate movement. The development of procambial strands in very young leaves was followed, and the subsequent differentiation of proto- and metaphloem examined in both lamina and sheath. In major bundles the first two or three series of protophloem cells differentiated acropetally into the leaf and they or their crushed remnants could be recognized at all levels. A further three or four series of protophloem cells differentiated basipetally, as did the protophloem of all minor bundles and the metaphloem. The basipetal differentiation of the bulk of the phloem combined with crushing of older cells resulted in acute constriction or even complete local blockage of the functional phloem in the active meristematic region. This constriction of the phloem would tend to divert assimilates into the dividing cells both from the stem below and from the mature upper portion of the leaf. No constriction was found at the base of a mature sheath.     

COMPARATIVE FOLIAR HISTOGENESIS IN ACORUS CALAMUS AND ITS BEARING ON THE PHYLLODE THEORY OF MONOCOTYLEDONOUS LEAVES

A comparative histogenetic investigation of the unifacial foliage leaves of Acorus calamus L. (Araceae; Pothoideae) was initiated for the purposes of: (1) re-evaluating the previous sympodial interpretation of unifacial leaf development; (2) comparing the mode of histogenesis with that of the phyllode of Acacia in a re-examination of the phyllode theory of monocotyledonous leaves; and (3) specifying the histogenetic mechanisms responsible for morphological divergence of the leaf of Acorus from dorsiventral leaves of other Araceae. Leaves in Acorus are initiated in an orthodistichous phyllotaxis from alternate positions on the bilaterally symmetrical apical meristem. During each plastochron the shoot apex proceeds through a regular rhythm of expansion and reduction related to leaf and axillary meristem initiation and regeneration. The shoot apex has a three- to four-layered tunica and subjacent corpus with a distinctive cytohistological zonation evident to varying degrees during all phases of the plastochron. Leaf initiation is by periclinal division in the second through fourth layers of the meristem. Following inception early growth of the leaf primordium is erect, involving apical and intercalary growth in length as well as marginal growth in circumference in the sheathing leaf base. Early maturation of the leaf apex into an attenuated tip marks the end of apical growth, and subsequent growth in length is largely basal and intercalary. Marked radial growth is evident early in development and initially is mediated by a very active adaxial meristem; the median flattening of this leaf is related to accentuated activity of this meristematic zone. Differentiation of the secondary midrib begins along the center of the leaf axis and proceeds in an acropetal direction. Correlated with this centralized zone of tissue specialization is the first appearance of procambium in the center of the leaf axis. Subsequent radial expansion of the flattened upper leaf zone is bidirectional, proceeding by intercalary meristematic activity at both sides of the central midrib. Procambial differentiation is continuous and acropetal, and provascular strands are initiated in pairs in both sides of the primordium from derivatives of intercalary meristems in the abaxial and adaxial wings of the leaf. Comparative investigation of foliar histogenesis in different populations of Acorus from Wisconsin and Iowa reveals different degrees of apical and adaxial meristematic activity in primordia of these two collections: leaves with marked adaxial growth exhibit delayed and reduced expression of apical growth, whereas primordia with marked apical growth show, correspondingly, reduced adaxial meristematic activity at equivalent stages of development. Such variations in leaf histogenesis are correlated with marked differences in adult leaf anatomy in the respective populations and explain the reasons for the sympodial interpretation of leaf morphogenesis in Acorus and unifacial organs of other genera by previous investigators. It is concluded that leaf development in Acorus resembles that of the Acacia phyllode, thereby confirming from a developmental viewpoint the homology of these organs. Comparison of development with leaves of other Araceae indicates that the modified form of the leaf of Acorus originates through the accentuation of adaxial and abaxial meristematic activity which is expressed only slightly in the more conventional dorsiventral leaf types in the family.     

Gentianella tumailica (Gentianaceae) – A new species from cold deserts of northwest Himalaya,India

A new species of Gentianella, G. tumailica sp. nov., from Tumail in the Kargil district of Ladakh, northwest Himalaya, India is described and illustrated. This novelity is morphologically similar to the sympatric G. stoliczka in inflorescence pattern, calyx and corolla shapes, sagitate anthers, more or less rounded seeds, but differs in smaller size of vegetative and floral structures, larger basal leaves, few cauline leaves, leaf apex obtuse to rounded, calyx lobes unequal (2 longer, 3 shorter), inflorescence enveloped by 4 foliaceous bracts, capsule elliptic to oblong and seed coat smooth. In addition, a diagnostic key to all Indian species of Gentianella is presented.     

Todea from the Lower Cretaceous of western North America: implications for the phylogeny, systematics, and evolution of modern Osmundaceae

The first fossil evidence for the fern genus Todea has been recovered from the Lower Cretaceous of British Columbia, Canada, providing paleontological data to strengthen hypotheses regarding patterns of evolution and phylogeny within Osmundaceae. The fossil consists of a branching rhizome, adventitious roots, and leaf bases. The dictyoxylic stem has up to eight xylem bundles around a sclerenchymatous pith. Leaf traces diverge from cauline bundles in a typical osmundaceous pattern and leaf bases display a sheath of sclerenchyma around a C-shaped xylem trace with 2-8 protoxylem strands. Within the adaxial concavity of each leaf trace, a single sclerenchyma bundle becomes C-shaped as it enters the cortex. The sclerotic cortex is heterogeneous with an indistinct outer margin. The discovery of Todea tidwellii sp. nov. reveals that the genus Todea evolved by the Lower Cretaceous. A phylogenetic analysis combining morphological characters of living and extinct species with a previously published nucleotide sequence matrix confirms the taxonomic placement of T. tidwellii. Results also support the hypothesis that Osmunda s.l. represents a paraphyletic assemblage and that living species be segregated into two genera, Osmunda and Osmundastrum. Fossil evidence confirms that Osmundaceae originated in the Southern Hemisphere during the Permian, underwent rapid diversification, and species extended around the world during the Triassic. Crown group Osmundaceae originated by the Late Triassic, with living species appearing by the Late Cretaceous.     

Regulation of extent of vegetative development of the maize shoot meristem

In maize plants ( Zea mays L.), the extent of vegetative development in the shoot is precisely regulated such that the apical meristem produces a predictable number of leaves before converting to tassel development. In previous experiments using shoot apex culture, we showed that the developmental program that limits vegetative development in maize is not intrinsic to the shoot apical meristem. Rather, the meristem receives information from elsewhere in the plant and responds by either continuing leaf initiation or becoming determined for determinate growth and forming an inflorescence, the tassel. Here we examine leaf primordia as potential sources for that information using shoot apex culture. Our results show that the presence of the four to six youngest leaf primordia on the shoot apex is sufficient to provide such information. The ability to reset shoot development by meristem culture also allows us to examine the basis for expression of a specific phenotype at a particular developmental stage. We found that the mutation hcf106 , which is typically expressed only during seedling stages, is not re-expressed when the shoot morphogically has regained a juvenile phase.     

The Vascular Pattern of a Rhizomatous Ginger (Alpinia speciosa L. Zingiberaceae). 2. The Rhizome

The vascular system in the underground rhizome of Alpinia speciosaL. (Zingiberaceae) is seen to be arranged in three distinctzones. (1) An inner system of ‘scattered’ vascularbundles which serial cinematography reveals to have an axialpattern conforming to the basic ‘palm’ configuration(a system of upwardly branching leaf traces with interconnections).(2) An intermediate zone comprising a thin perforated cylinderof anastomosing vascular strands having direct contact withboth roots and inner system bundles. (3) An outer system offreely-anastomosing vascular bundles. Connexion of outer andinner system occurs in the form of extensive bridging from innersystem leaf traces as they depart obliquely between the outersystem network. The interrelation of the three systems, plus root and branchinsertion, is illustrated by means of diagrammatic three-dimensionalreconstructions. The intermediate zone is intimately associatedwith root insertions and with the inner system, and is shownto obliviate potential bottlenecks at the point of lateral branchinsertion in this sympodial rhizome system. A comparison ismade with other monocotyle-donous vascular systems. Alpinia speciosa L., shell ginger, rhizome, vascular anatomy     

CAULINE VASCULATURE AND LEAF TRACE PRODUCTION IN MEDULLOSAN PTERIDOSPERMS

Medullosa and Sutcliffia specimens from the Paleozoic of North America and Europe are examined to determine the architecture of the cauline vasculature and mode of leaf trace production. Emphasis is placed on the identification and characterization of protoxylem strands and their relationship to leaf trace production. Organization of the primary xylem varies from a single protostele to a dissected stele composed of two to many more or less independent bundles. In Medullosa the bundles of primary xylem are each surrounded by secondary xylem, forming separate segments of vascular tissue (‘steles’ of previous workers). These vascular segments may divide and fuse at different levels in the stem. A definite number of protoxylem strands occur near the periphery of the primary xylem. The protoxylem strands divide at intervals producing protoxylem to the departing leaf traces. Leaf traces thus formed arise from all the vascular segments in a coordinated and predictable way and pass outward through emission areas in the secondary xylem. This type of cauline vascular architecture is compared to that of other seed plants. The vascular system of Medullosa stems is interpreted as a dissected monostele. Sympodial vascular architecture has apparently evolved from a protostele separately within the medullosan pteridosperms.     

barren inflorescence2 regulates axillary meristem development in the maize inflorescence

Organogenesis in plants is controlled by meristems. Shoot apical meristems form at the apex of the plant and produce leaf primordia on their flanks. Axillary meristems, which form in the axils of leaf primordia, give rise to branches and flowers and therefore play a critical role in plant architecture and reproduction. To understand how axillary meristems are initiated and maintained, we characterized the barren inflorescence2 mutant, which affects axillary meristems in the maize inflorescence. Scanning electron microscopy, histology and RNA in situ hybridization using knotted1 as a marker for meristematic tissue show that barren inflorescence2 mutants make fewer branches owing to a defect in branch meristem initiation. The construction of the double mutant between barren inflorescence2 and tasselsheath reveals that the function of barren inflorescence2 is specific to the formation of branch meristems rather than bract leaf primordia. Normal maize inflorescences sequentially produce three types of axillary meristem: branch meristem, spikelet meristem and floral meristem. Introgression of the barren inflorescence2 mutant into genetic backgrounds in which the phenotype was weaker illustrates additional roles of barren inflorescence2 in these axillary meristems. Branch, spikelet and floral meristems that form in these lines are defective, resulting in the production of fewer floral structures. Because the defects involve the number of organs produced at each stage of development, we conclude that barren inflorescence2 is required for maintenance of all types of axillary meristem in the inflorescence. This defect allows us to infer the sequence of events that takes place during maize inflorescence development. Furthermore, the defect in branch meristem formation provides insight into the role of knotted1 and barren inflorescence2 in axillary meristem initiation.     

Non-axillary branching in the palms Eugeissona and Oncosperma (Arecaceae)

FISHER, J. B., GOH, C. J. & RAO, A. N., 1989. Non-axillary branching in the palms Eugeissona and Oncosperma (Arecaceae). The south-east Asian palms, Eugeissona (Calamoideae) and Oncosperma (Arecoideae) are multiple-stemmed. The morphology and development of branching in two species of each genus were examined in Singapore, Borneo, and the Malay Peninsula. Cultivated seedling and adult plants of 0. tigillarium were also observed in Florida. A new shoot arises most often from a longitudinal abaxial groove at the base of an enclosing leaf sheath. In some instances, especially in E. tristis , the enclosing leaf has two equal, adjacent grooves such that any distinction between an original mother shoot and a lateral daughter shoot is impossible. No axillary buds occur in Eugeissona which is hapaxanthic. In Oncosperma , which is pleonanthic, axillary buds are absent from young pre-flowering stems, but an inflorescence bud occurs in the axil of each leaf in older aerial stems. Early ontogenetic stages of vegetative branching, as seen in sectioned apices, indicate that a new vegetative shoot is present on the abaxial base of the first (youngest) leaf primordium. There is no ontogenetic evidence for the displacement of an originally axillary meristem as previously described for the palm Salacca (Calamoideae). Shoot development in Eugeissona is interpreted as a putative dichotomy of the apical meristem in which the meristem centres commonly develop unequally. In Oncosperma the smaller sucker bud meristem may be described as an abaxial leaf base bud, but ontogenetic variations indicate this form of branching is close to dichotomous branching. These new examples of non-axillary branching are compared to similar cases previously reported for palms and other monocotyledons.