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.     

THE LEPIDOPHYTIC AFFINITIES OF THE GENUS CHINLEA AND OSMUNDITES WALKERI

Chinlea campii Daugherty and Osmundites walkeri Daugherty are species of petrified stems from the Upper Triassic Chinle Formation of Arizona that were described as members of the fern family Osmundaceae. Investigation of additional material indicates that the two species are conspecific and belong to the Lepidophyta. The stems are radially symmetric and have an ectophloic siphonostele in which the xylem cylinder is thick and deeply furrowed. Internal pressure against the xylem cylinder caused by the lateral expansion of the pith in some stems produces what appears in transverse section to be a ring of up to 60 separate xylem strands. Leaf traces are small, terete, collateral and have exarch xylem. They are arranged in a tight spiral. Adventitious roots, secondary xylem, and secondary cortex are lacking. The stems are classified under the binomial Chinlea campii, and other axes that have similar cortical anatomy but in which all vascular tissues have decayed are treated as Chinlea sp. Both types of stems are interpreted as ephemeral aerial shoots of an herbaceous plant. Of the known fossil Lepidophyta, Chinlea is most similar to Pleuromeia and Nathorstiana, but it differs from each of these genera in a number of respects and is therefore included in Lepidophyta incertae sedis.     

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.     

RHABDOXYLON AMERICANUM SP. N., A STRUCTURALLY SIMPLE FERN-LIKE PLANT FROM THE UPPER PENNSYLVANIAN OF ILLINOIS

A new species of the genus Rhabdoxylon Holden (1960), an anatomically simple plant of presumed fern or fern-like affinities, is described from a coal ball petrifaction found in the Upper Pennsylvanian of southern Illinois. The new species, R. americanum, is based upon five specimens consisting of stems bearing spirally arranged leaves and numerous randomly distributed adventitious roots. The haplostelic stems branch by equal dichotomies and bear foliar traces which arise as unequal dichotomies of the stele. Leaf traces possess a circular outline in cross section and one adaxial protoxylem strand. The characteristics of exclusively primary tissues, diarch adventitious roots, centrarch haplosteles with simple scalariform pitting, and the nature and arrangement of the leaf traces, suggest that Rhabdoxylon represents a fern or fern-like plant rather than a representative of the Rhyniophytina or Trimerophytina. At present it is not possible to determine whether the simple structure of Rhabdoxylon has come about through phyletic reduction or represents a primitively simple condition.     

A NEW STRUCTURALLY PRESERVED PENNSYLVANIAN CORDAITEAN POLLEN ORGAN

Permineralized specimens of the pollen organ Gothania (Hirmer) consist of a primary axis bearing pollen cones in the axils of bracts that are four ranked. The bilaterally symmetrical primary axis consists of a uniform parenchymatous pith surrounded by up to 15 endarch-mesarch axile bundles. The cortex is two-parted and consists of an inner zone of subepidermal fibers. Bract traces arise from the ends of the ellipsoid stele. Traces to the cones are derived from the open ends of the stele, and at higher levels form a centrarch-medullated vascular system. Each pollen cone is constructed of up to 25 helically arranged scales, each vascularized by a single trace that may dichotomize. Scales are elongate and broad, and histologically composed of mesophyll parenchyma and fibrous layers. Stomata are restricted to the adaxial surface between rows of fibers. Up to 10 distal scales may be fertile, each with 4 elongate pollen sacs at the tip. Large monosaccate grains of the Felixipollenites-type are densely packed in each pollen sac. The well-preserved specimens of Gothania provide an opportunity to compare this genus with pollen cones assigned to the genus Cordaianthus, and to relate isolated plant organs to the Cordaitales.     

VASCULAR CONNECTION BETWEEN LATERAL ROOTS AND STEM IN THE OPHIOGLOSSACEAE

The vascular connection between lateral roots and stem in the Ophioglossaceae and in two leptosporangiate fern species was examined. Two types of connections were found: “gradual” connections, which resemble leaf traces in ontogeny and morphology, and “abrupt” connections, which resemble the connections between lateral roots and their parent roots. Gradual root-stem connections occur in the genera Ophioglossum and Helminthostachys and in Woodwardia virginica. They are initiated in shoot apices distal to the level where cauline xylem elements mature. They resemble leaf traces in being provascular (procambial) strands that connect the cauline stele with the future vasculature of lateral appendages. As with leaf traces, gradual connections are part of the provascular and, later, protoxylem continuity between stems and lateral appendages. Gradual connections have many features in common with leaf traces, and the term root trace is applicable to them. The order of radial maturation of the primary xylem in gradual connections varies in different parts of the connections. It is endarch near the intersection with the cauline stele and exarch where the connections intersect root steles. Gradual connections resemble the transition regions of certain seed plants where protoxylem is also continuous from stem to root and the order of maturation is found to change continuously from stem to root. Abrupt connections occur in Botrychium and Osmunda cinnamomea. They develop in shoot apices at levels where cauline xylem is mature or maturing. The mature xylem does not dedifferentiate, so provascular and protoxylem continuity of the kind found in root traces does not occur. Also, reorientation of the order of maturation does not occur in abrupt connections. Xylem connectors are found in the region where radially oriented elements of the connections abut the longitudinally oriented cauline elements. Abrupt connections resemble the connection of secondary roots with their parent root systems since xylem connectors and the lack of continuity are also features found in these vascular systems. The resemblance of the vascular pattern of the fern root trace to the transition region of seed plants suggests that the radicle is more closely comparable to the cladogenous roots of pteridophytes than hitherto supposed.     

The architecture of Zeylanidium olivaceum (Podostemaceae) inferred from the structure of the primary shoots

Zeylanidium olivaceum (Podostemaceae-Podostemoideae) is the only crustose-rooted species of the genus that still develops prominent primary shoots from the seedling in addition to the secondary (root-borne) shoots forming the clonal plant body. The primary shoots are articulated into an up to 8.5 cm long and 4 mm thick stalk (hypocotyl) and a copiously foliated paint-brush-like shoot which is sympodially branched in the form of a helicoid cyme. The helicoid branching pattern indicates a transversal prophyll position, typical of the dicotyledons, but replaced in most other Podostemoideae by a median prophyll position. The short stems within the leafy head do not separate, but are fused to a dense aggregate (coenosome). Branches are mainly vegetative with a rosette of about 20 elongate subulate leaves. The primary shoots branch in the vegetative stage and thus differ from other Podostemoideae where ramification is confined to the floriferous shoots. The leaves adhere together at the base, forming an apical furrow-like hollow surrounding the shoot tip. The tiny shoot apex is one-layered, radially symmetrical, and develops leaf primordia in a decussate pattern. The erect primary shoots thus differ from the distichously foliated plagiotropic secondary shoots by the decussate phyllotaxis, and by the presence of more than 20 leaves on a shoot as compared to the about six leaves on the vegetative and floriferous secondary shoots. The features observed in the primary shoots are interpreted as primitive as compared to those of the secondary shoots. Z. olivaceum is thus characterised by heterobathmy, i.e., the occurrence of plesiomorphic (primary shoots) and apomorphic features (secondary shoots). The primary shoots exhibit primitive features that apparently have been lost in secondary and primary shoots of most other members of subfamily Podostemoideae.     

AUREALCAULIS CROSSII GEN. ET SP. NOV., AN ARBORESCENT,OSMUNDACEOUS TRUNK FROM THE FORT UNION FORMATION (PALEOCENE), WYOMING

Aurealcaulis crossii gen. et sp. nov., is based on permineralized trunks of an osmundaceous tree fern from the Paleocene Fort Union Formation from near Bitter Creek Station of southwestern Wyoming. This new species is characterized by centripetal (exarch) development of its xylem strands which form part of the leaf traces. Most of the leaf traces depart the stele as two segments that fuse into a single C-shaped petiole vascular strand outside of the outer cortex. Stipular expansions of the petiole bases of this species lack sclerenchyma, and roots arise from the lateral edges of leaf traces in the inner cortex. The family Osmundaceae and subfamily Osmundoideae are slightly emended to accept genera assignable to this family and subfamily with exarch protoxylem in their steles. Foliage similar to Osmunda greenlandica (Heer) Brown, which is possibly the leaf form of A. crossii, occurred next to an axis of this species which was in growth position. This axis was anchored in a lignite suggesting that this species grew under swampy conditions. Aurealcaulis crossii is the first arborescent member of the Osmundaceae of Tertiary age and the second arborescent form in this family reported from the Northern Hemisphere.     

A THREE-DIMENSIONAL RECONSTRUCTION OF THE VASCULAR SYSTEM TO THE LODICULES,ANDROECIUM, AND GYNOECIUM OF A FERTILE FLORET OF PANICUM DICHOTOMIFLORUM (GRAMINEAE)

A three-dimensional reconstruction of a fertile floret stele of Panicum dichotomiflorum approaching anthesis was made by a new technique using superimposition of tracings of 80, 1-μm thick serial sections, cleared tracing film, and mounting adhesive. From a collateral bundle, which also served as the median trace to the fertile lemma, most of the vascular tissue branched adaxially and horizontally to become the sole vascular supply to the two lodicules, three stamens, and pistil. The xylem branched at a low level to form a broad and long vessel plexus. The phloem branched at a higher level to overlay the vessel plexus on the right and left with an arc of horizontal sieve tubes in a phloem plexus. Those sieve tubes and vessels which rose after branching from the horizontal plexi assumed a more vertical course in the floret stele. Traces to the right and left lodicules arose from the lower abaxial portions of the flanks of the floret stele. Vessels ascended vertically from the xylem plexus and passed through the phloem plexi and joined with the sieve tubes there to exit at the same level and become the right and left lodicule traces. The vascular tissues to the three filament traces arose from different higher levels of the stele. The sieve tubes for the median filament trace arose vertically from the abaxial side between but above the lodicule traces. At higher levels the sieve tubes for the lateral filaments rose from the horizontal arcs of the flanks of the stele and departed it tangentially. The vessels destined to the filament traces arose in the center of the floret stele from adaxial portions of the horizontal plexus, ascended between the arcs of phloem, exited the stele simultaneously above the phloem of the traces, and followed the courses of their respective sieve tubes. The adaxially displaced apex of the floret stele then contained the vascular tissue related to the pistil. All the sieve tubes and vessels of the floret stele were embedded in a matrix of intermediary cells. The peripheral intermediary cells associated with the vessel plexus were xylem transfer cells with pronounced wall ingrowths. At higher levels in the floret stele, intermediary cells in scattered locations near sieve tubes or vessels had less conspicuous wall ingrowths. No preferred orientation of transfer cells with any particular trace was noted.     

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.     

Observations on phyllotaxis, stelar morphology, the shoot apex and gemmae of Lycopodium lucidulum Michaux (Lycopodiaceae)

Phyllotaxis in Lycopodium lucidulum consists of low alternating spirals, with the adult shoots corresponding to a system of 5 + 5 contact parastichies in which there are ten orthostichies. Each major stelar lobe is a sympodium of the leaf traces of two orthostichies and each lobe has two mesarch xylem poles, Differentiation of both the procambium and xylem of the leaf traces is bidirectional, that is differentiation first commences in the leaf base and then is acropetal into the leaf and basipetal into the stem. Furthermore, the procambium of the axis does not extend above that of the youngest leaf primordium and the axial procambium is in part a composite of that of the leaf traces. Thus, it is concluded that the stele in this taxon is not a strictly cauline structure. The shoot apex consists of four zones—a zone of surface initials, a zone of subsurface initials, a peripheral zone and a rib meristem. This zonation pattern is essentially the same as that of the seed plants. From their inception, gemma primordia also exhibit shoot apical zonation and are entirely different from leaves in their subsequent growth pattern and vascularization. Although the gemmae occupy leaf sites in the phyllotactic sequence, they are interpreted as arrested stem dichotomies on the basis of their development and vascular system.     

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.     

The stele – a developmental perspective on the diversity and evolution of primary vascular architecture

The stele concept is one of the oldest enduring concepts in plant biology. Here, I review the history of the concept and build an argument for an updated view of steles and their evolution. Studies of stelar organization have generated a widely ranging array of definitions that determine the way we classify steles and construct scenarios about the evolution of stelar architecture. Because at the organismal level biological evolution proceeds by changes in development, concepts of structure need to be grounded in development to be relevant in an evolutionary perspective. For the stele, most traditional definitions that incorporate development have viewed it as the totality of tissues that either originate from procambium – currently the prevailing view – or are bordered by a boundary layer (e.g. endodermis). Consensus between these two perspectives can be reached by recasting the stele as a structural entity of dual nature. Following a brief review of the history of the stele concept, basic terminology related to stelar organization, and traditional classifications of the steles, I revisit boundary layers from the perspective of histogenesis as a dynamic mosaic of developmental domains. I review anatomical and molecular data to explore and reaffirm the importance of boundary layers for stelar organization. Drawing on information from comparative anatomy, developmental regulation, and the fossil record, I propose a stele concept that integrates both the boundary layer and the procambial perspectives, consistent with a dual nature of the stele. This dual stele model posits that stelar architecture is determined at the apical meristem by two major cell fate specification events: a first one that specifies a provascular domain and its boundaries, and a second event that specifies a procambial domain (which will mature into conducting tissues) from cell subpopulations of the provascular domain. If the position and extent of the developmental domains defined by the two events are determined by different concentrations of the same morphogen (most likely auxin), then the distribution of this organizer factor in the shoot apical meristem, as modulated by changes in axis size and the effect of lateral organs, can explain the different stelar configurations documented among tracheophytes. This model provides working hypotheses that incorporate assumptions and generate implications that can be tested empirically. The model also offers criteria for an updated classification of steles in line with current understanding of plant development. In this classification, steles fall into two major categories determined by the configuration of boundary layers: boundary protosteles and boundary siphonosteles, each with subtypes defined by the architecture of the vascular tissues. Validation of the dual stele model and, more generally, in-depth understanding of the regulation of stelar architecture, will necessitate targeted efforts in two areas: (i) the regulation of procambium, vascular tissue, and boundary layer specification in all extant vascular plants, considering that most of the diversity in stelar architecture is hosted by seed-free plants, which are the least explored in terms of developmental regulation; (ii) the configuration of vascular tissues and, especially, boundary layers, in as many extinct lineages as possible.     

波温苏铁(Bowenia spectabilis)营养器官的解剖结构研究

报道了波温苏铁Bowenia spectabilis Hook.ex Hook. f）根、茎、叶的解剖结构.根的初生结构由表皮、皮层和中柱三部分组成,为二原型木质部.茎具大量薄壁组织,薄壁细胞富含淀粉粒,维管束为外韧并生.叶柄中含有5-8束维管束,呈弧形排列.羽片叶角质层厚,有小叶脉产生,气孔主要分布在下表皮.根、茎、叶木质部中的管胞主要是螺纹和孔纹管胞,有少量纤维分化;茎中管胞的侧壁呈现凹凸不平,部分管胞具有分枝或分叉现象.     

ANATOMY OF SEEDLING ROOTS OF PSEUDOTSUGA MENZIESII

The seedling root system of Pseudotsuga menziesii (Mirb.) Franco consists of the primary root, active long laterals, long laterals that become mycorrhizal, and short roots that may or may not become mycorrhizal. Numerous adventitious roots arise from the pericycle in young roots and from the vascular cambium and pericycle in older roots following pruning. All actively growing apices have a single plate of initials, a complex zonation of mother cells, and a similar pattern of primary tissue differentiation. Short roots and mycorrhizal short roots have 2 plates of initials, one producing the stele and the other the root cap and cortex, and differentiation occurs close to the apex. Primary and adventitious roots are usually triarch, while long laterals are usually diarch as are all short roots. The latter lack secondary xylem, but mycorrhizal short roots may produce a small amount of secondary phloem.     

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.     

Relationship of Auxin Transport to Branch Dimorphism in Cordyline, a Woody Monocotyledon

Lanolin containing ³H-IAA was applied to apical cut ends of stem segments and decapitated plants of Cordyline terminalis, a monocotyledon possessing true secondary growth. Distribution of extracted label showed that: 1) in horizontal stems up to 7 times as much label accumulates in the lower surface compared to the upper surface, and this ratio increases with distance from the cut apical surface; 2) in upright stems most label (62%) occurs in the cambial and cortical regions, external to the primary and secondary vascular tissues; and 3) in upright stems having the cambium and cortical regions removed by a girdle, label accumulates above the girdle (c. 10 times greater than the control). These data are in accord with a theory of branch dimorphism derived from morphological studies, which suggested that high auxin levels initiate and maintain rhizomes and low levels initiate leafy shoots.     

Preliminary Studies of Root-Stem Transition in Brassica napus L.

Seedlings of Brassica napus L. 2–11 days after germination were used. However, the most investigation was concentrated on the 6-day old seedlings. The primary root has a diarch protostele, the two groups of primary phloem alternate with the primary xylem. At higher level, the metaxylem is gradually differentiated in a lateral direction. Being coincident with this changes of the metaxylem, the groups of phloem cell are extended. The stele of the lower hypocotyl is root-like and has no pith. In the middle hypocotyl, there is a further lateral differentiation of the metaxylem. At the higher level, four metaxylem arms appear and the groups of phloem are extended circumferentially to form two crescent shaped sectors. In the upper hypocotyl below 0.2 cm of the cotyledonary node, a central pith has been formed which separates the differentiating primary xylem into two distinct units. At a slightly higher level, each primary phloem divides into two small groups, at this time, each xylem unit and the two adjacent groups of phloem constitute a cotyledonary trace. The foliar traces of the first two foliage leaves appear in the inter-cotyledonary plane between the vascular elements of the cotyledonary traces. At this level, the vascular tissue of the hypocotyl forms a siphonostele made up of two cotyledonary traces and the two foliage leaves, where the root-stem transition has nearly been completed, while the endarch condition is not attained in the hypocotyl. At incresing distances from the cotyledonary node upwards, in the cotyledonary petiole, the protoxylem occupies a more and more adaxial position and the metaxylem a more and more abaxial direction and, thus, the endarch condition is attained. The primary system of the root, hypocotyl, and cotyledons forms a complete circular system, the plumular vascular elements are directly connected by secondary elements formed by the cambium in the region of the hypocotyl. As for the results mentioned above, the authers have not detected that the primary xylem has a rotation of 180˚, as described by Van Tieghem.     

COMPARATIVE MORPHOLOGY OF THE PRIMARY VASCULAR SYSTEMS IN SOME SPECIES OF ROSACEAE AND LEGUMINOSAE

The structural patterns of the primary vascular systems in some species of Leguminosae and Rosaceae have been determined by tracing the longitudinal course of the vascular bundles in terminal stem segments. These systems are interpreted as consisting of sympodia. Each sympodium is composed of an axial bundle which is continuous through the length of the segment and from which arise trace bundles that supply leaves and axillary buds. A compact arrangement of vascular bundles seems to correlate with the woody habit. Regardless of the degree of compactness of the primary vascular system, the structural identity of the individual sympodia is maintained. The total number of vascular bundles at a particular level is related to the number of axial bundles in the system, the number of traces per leaf and per axillary bud, and the number of internodes traversed by the traces prior to entering a lateral appendage. Shrubs and trees have more vascular bundles than herbs. Data from this study and the literature indicate that the vascular system is predominantly of the open type in dicotyledonous plants which have helically arranged leaves and, further, that in such plants with a 3-trace, trilacunar nodal structure, the number of sympodia coincides with the number of orthostichies (which is also the denominator of the phyllotactic fraction). In open systems leaf gaps cannot be morphologically delimited. Because of the resemblance of the open type of angiosperm vascular system to that of certain gymnosperms, previously interpreted to have evolved from a protostele, we suggest that the eustele of angiosperms is homologous with the stele of gymnosperms. We believe, also, that angiosperms, like gymnosperms, are probably not characterized by leaf gaps of filicinean type. We provide, furthermore, a rationale for the view that the axial bundle of a sympodium is a cauline structure.