Contributions to the Morphology of Some Species of Microsorium

Morphology of eleven epiphytic and rupicaulous species of Microsoriumis described. The paleae in the genus are either peltate withthe basal region developing secondarily as a hood over the stalk,or basally attached with auricles on either side of the stalk.The auricles in M. hancockii and M. pteropus develop from singleinitial cells adjacent to the stalk, while in the others nospecialized initial cells occur. Marginal and terminal glandularhairs occur on the paleae, except in M. hancockii and M. pteropusin which marginal hairs are absent. Slender sclerenchyma strands are scattered profusely in theground tissue of the rhizome. The stelar cylinder is dictyostelicand is dissected by lacunae into cylindrical vascular bundles.Leaf traces are multiple strands originating as branches fromthe dorsal median vascular bundle of the stelar cylinder andthe one next to it on each side. Two or three closely placedvascular bundles of the rhizome constitute the vascular connexionto each branch of the rhizome. Venation of the leaf lamina is reticulate with most of the free-endingveinlets entering foliar hydathodes. The juvenile leaves bearhairs similar to the pro-thallial hairs and are spatulate witha medianly placed forked vein. Sori are generally punctiform,but in M. hancockii and M. pteropus spread slightly over theveins, often forming elongated coenosori. Uniseriate (multiseriatein M. rubidum), multicellular paraphyses occur in all speciesexcept M. scolopendria. The spores are monolete and either psilateor granulate. The prothalli develop from 3-5 cells long germ filaments inwhich the anterior cells divide longitudinally and form an ameristicprothallial plate. An apical meristematic cell is formed later,and a cordate prothallus is developed, except in M. hancockiiand M. pteropus in which a definite meristem is never formedand the prothalli are ribbon-shaped and branched. The cordateprothalli possess polypodiaceous hairs: the ribbon-shaped onesare more or less naked and devoid of any midrib. The chromosome number in the species is n = 36 (zn = 72).     

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.     

ANATOMICAL STUDIES OF CYATHEA AND TRICHIPTERIS (CYATHEACEAE)

Comparative anatomical studies of the mature stems of two species each of Trichipteris and Cyathea (Cyatheaceae) are described. The outermost boundary of the stem is typically a two-layered hypodermis. Mucilage-sac cells are randomly distributed in all parenchymatous areas of the stem and form articulated laticifer systems. Localized areas of sclerenchyma tissue occur in the cortex of both T. microphylla and C. suprastrigosa. All species studied possess medullary bundles, whereas cortical bundles are found only in T. trichiata. Accessory bundles occasionally are associated with indentations in the internal stelar sheath of T. trichiata. The stelar pattern in each genus is a dictyostele and consists of individual meristeles. Distinctive cubical cells typically occur wherever sclerenchymatous fibers and parenchyma cells abut one another. Tangential cells occur within the primary phloem of each meristele, and occasionally within the larger accessory bundles. The primary xylem of the adventitious roots is typically diarch, although triarch and tetrarch xylem may occur. Leaf traces and petiole strands are similar anatomically to the accessory bundles. Based upon this study Trichipteris and Cyathea show striking anatomical similarities, and appear to be closely-related taxa.     

Vascular Organization and some Aspects of the Morphology of the Rhizome of Gymnogrammitis dareiformis

Gymnogrammitis dareiformis, the taxonomically controversialdavalliaceous fern has a parenchymatous rhizome, in the groundtissue of which groups of 1–16 thick-walled cells (withpeg-like protrusions on inner walls) are irregularly scattered.Paleae clothing the rhizome are basally attached, gland-tippedand bearing unicellular marginal hairs. The vascular cylinderis a radially-symmetric dictyostele dissected by spirally-arrangedleaf gaps into slender reticulated meristeles. Some of the dorso-laterallyplaced leaves alone are fully developed; most other leaves aresuppressed and some are highly reduced (the larger reduced leavesappear as protrusions on the rhizome and have a well-formedleaf base). The leaf trace of developed as well as the largerreduced leaves is a channel-shaped loose reticulum of four vascularstrands; the trace of the reduced leaves is smaller and endsblindly at the leaf base. The leaf trace of the smaller reducedleaves is vestigial and represented often by only a pair ofvascular strands fusing into one and ending blindly in the cortexof the rhizome. The leaf trace of suppressed leaves fuses backwith the stelar cylinder, forming a convex reticulum bridgingthe sides of the leaf gap. It is suggested that the characteristic stelar organizationof the Davalliaceae is derived by suppression of leaves froma radiallysymmetric dictyostele with spirally-arranged leafgaps as found in Nephrolepis and that Gymnogrammitis with itsreduced and suppressed leaves indicates the process of transition.The creeping solenostelic rhizome with two-ranked leaf arrangementcould be derived from an erectgrowing dictyostelic one by supppressionof leaves.     

MORPHOLOGICAL STUDIES OF THE NYMPHAEACEAE SENSU LATO. XVII. FLORAL ANATOMY OF ONDINEA PURPUREA SUBSPECIES PURPUREA (NYMPHAEACEAE)

Classification and phylogeny of the Nymphaeaceae are unresolved. This study provides floral anatomical data that will assist in elucidating generic interrelationships and systematic relationships to other taxa of angiosperms. The floral anatomy of Ondinea purpurea den Hartog subsp. purpurea has been examined utilizing light microscopy. The peduncle possesses stelar vascular bundle complexes and cortical vascular bundles. Cortical bundles terminate within the peduncle. Each bundle complex consists of 2 collateral bundles on the same radius, the inner bundle inverted; 2 protoxylary lacunae occur yet differ in structure and function. Progressing acropetally, the inner xylary lacunae become discrete mesarch strands surrounded centrifugally by a vascular cylinder formed by divisions and anastomosing of the bundle complexes. Together these become the massive receptacular vascular plexus. The plexus provides collateral traces to the floral organs. Each sepal receives 3 traces that separate from the plexus as 1–3 lateral traces. Petals are absent and no vestigial petal traces have been observed. Distally, the plexus forms several large strands of connate gynoecial and androecial traces termed the principal vascular bundles (PVBs). Ventral veins separate from the PVBs and the latter extend acropetally through the outer ovary wall. Branches of the ventrals and PVBs contribute to septal vascular reticula from which each ovule is supplied by one vascular bundle. Each stamen receives 1 trace from branches of the PVBs. The ventrals and PVBs terminate within the carpellary lobes. A comparative anatomical study is offered that supports the inclusion of Ondinea in the Nymphaeaceae sensu stricto.     

Taxonomic differences among closely related pines Pinus sylvestris, P. mugo, P. uncinata, P. rotundata and P. uliginosa as revealed in needle sclerenchyma cells

The purpose of the present study was to test the taxonomic value of sclerenchyma in distinguishing Pinus sylvestris and P. mugo, P. uncinata, P. rotundata and P. uliginosa, all representing the subsection Sylvestres within the genus Pinus. Thirty-six samples were gathered in natural populations. Every sample was represented with 30 individuals, every individual with 10 brachyblasts. Three types of sclerenchymatic cells surrounding the resin canals and four between vascular bundles were distinguished. Relations among samples and taxa were verified using discriminant analysis and clustering based on Euclidean distances. The types of sclerenchymatic cells surrounding the resin canals and located between the vascular bundles differentiate the compared taxa when used as average frequencies but are extremely variable and do not allow the classification of every individual. The study demonstrated that the type of sclerenchymatic cells surrounding the resin canals and between the vascular bundles in needles could have an important taxonomic value in distinguishing the taxa of two-needle pines of the subsection Sylvestres in Europe at the population level. The distinguishing of individuals was difficult because of very high variation of sclerenchyma characters.     

COMPARATIVE STUDIES OF THE NODAL AND VASCULAR ANATOMY IN THE NEOTROPICAL CYATHEACEAE. III. NODAL AND PETIOLE PATTERNS; SUMMARY AND CONCLUSIONS

Comparative studies of the nodal and vascular anatomy in the Cyatheaceae are discussed as they relate to the taxonomy and phylogeny of the family. There is in the Cyatheaceae (excluding Metaxya and Lophosoria) a basic nodal pattern consisting of four major phases of leaf trace separations. Abaxial traces arise from the leaf gap margins, and the last abaxial traces from each side of the gap are larger and undergo numerous divisions. Distally adaxial traces separate from the gap margins, and the last adaxial traces are usually larger and undergo multiple divisions. In addition, medullary bundles frequently become petiole strands of the adaxial arc in the petiole. Rarely, cortical bundles form petiole strands in the abaxial arc in the petiole. Leaf gaps of the squamate genera of the Cyatheaceae are fusiform and possess prominent lateral constrictions which result from medullary bundle fusions and the separation of leaf traces. A characteristic petiole pattern is found in all members of the Cyatheaceae. There is an increase in the complexity of the petiole vascular tissue which results in a gradation from the undivided strand in Metaxya, to the three-parted petiole pattern in Lophosoria, and finally to the much-dissected petiole vascular tissue in the advanced genera. Nodal and vascular anatomy data basically support Tryon's phyletic scheme for the family. The Sphaeropteris-Alsophila-Nephelea line shows certain tendencies toward increased complexity of nodal and vascular anatomy, whereas the Trichipteris-Cyathea-Cnemidaria line shows the same anatomical and morphological characters in a direction of increased simplification or reduction.     

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.     

Plenasium xiei sp. nov. from the Cretaceous of Northeast China: Additional evidence for the longevity of osmundaceous ferns

A new species of the Osmundaceae, Plenasium xiei sp. nov., is herein described from the Cretaceous of Northeast China. The specimens examined here represent the earliest unequivocal record of the extant genus Plenasium in Eurasia based on fossil rhizomes. The rhizome consists of a central stem with a mantle of petiole bases and adventitious roots. The stem contains an ectophloic‐dictyoxylic siphonostele and a two‐layered cortex. The C‐shaped leaf trace bears two protoxylem bundles at the point of separation from the stele. The pith is heterogeneous. The parenchymatous inner cortex is thinner than the sclerenchymatous outer cortex. Lobed sclerenchyma bands occur at the adaxial sides of the stem xylem strands, in the concavity of the leaf trace, and along the adaxial side of the vascular bundles of the petiole base. In distal petiole portions, the sclerenchyma band splits into several groups in the transverse view. Sclerenchyma rings are heterogeneous with an abaxial sclerenchymatous arc of thick‐walled fibers. Numerous sclerenchyma strands of thick‐walled fibers appear in the petiolar inner cortex and the stipular wing. These fossils provide unambiguous evidence for the existence of subgenus Plenasium of modern Plenasium by at least the Late Cretaceous, demonstrating the longevity of this extant subgenus. Altogether the leaf and rhizome fossil records of Plenasium indicate that this genus was widely distributed across North America and Eurasia from the Early Cretaceous to the Early Cenozoic, followed by a range restriction to Eurasia in the Late Cenozoic. Extant Plenasium species are only known from East and Southeast Asia.     

A new tree fern stem,Heilongjiangcaulis keshanensis gen. et sp. nov., from the Cretaceous of the Songliao Basin,Northeast China: a representative of early Cyatheaceae

A new genus and species of Cretaceous Cyatheacean tree fern, Heilongjiangcaulis keshanensis gen. et sp. nov., is erected for several permineralized stems collected at the Keshan County in Songliao Basin, Heilongjiang Province, Northeast China. The new taxon is characterized by a dictyostelic, erect stem with dense multicellular scales and surrounded by persistent petiole bases and adventitious roots. The stem contains a central pith lacking medullary bundles, which is surrounded by a dictyostele, and the cortex externally. Each meristele of the dictyostelic ring is enclosed by a sclerenchyma sheath. The pith and cortex are parenchymatous. The proximal petiole bases present a frond trace composed of numerous meristeles, arranged in 1 abaxial and 2 adaxial arcs, with internally projecting bundles on the upper and lateral sides. The feature combination of the new genus is nearly identical to the anatomical structures of modern scaly genera of the Cyatheaceae apart from the absence of medullary bundles. It is interpreted as a primitive representative of early Cyatheaceae, that closely resembles the modern scaly genera, which suggests that in the Cretaceous, the tree ferns in this family were already in possession of most of the anatomical characteristics observed in extant taxa. The fossil records of the stems, petioles, and spores indicate that during the Jurassic and Cretaceous, the Northeastern region of Asia may have been one of the distribution centers of early Cyatheaceae.     

Comparative vegetative anatomy of Stanhopeinae (Orchidaceae)

Stanhopeinae are a group of tropical American orchids characterized by euglossine bee pollination and lateral inflorescences stemming from the bases of pseudobulbs. Leaves are hypostomatal, and all stomatal configurations are tetracytic. Chlorenchyma is homogeneous and characterized by fibre bundles in adaxial/abaxial or adaxial/median/abaxial positions. Collateral vascular bundles occur in a single row and feature phloic and xylic sclerenchymatous caps and thin-walled bundle sheath cells. Fibre bundles and vascular sclerenchyma are accompanied by stegmata containing conical silica bodies. Pseudobulbs have thick-walled turbinate epidermal cells and ground tissue of smaller, living assimilatory cells and larger, dead water-storage cells. Fibre bundles are usually absent but occur in several genera. Collateral vascular bundles show phloic sclerenchyma, but xylic sclerenchyma occurs only in die larger vascular bundles. Phloic and xylic sclerenchyma are associated with stegmata containing conical silica bodies. Roots are velamentous. Velamen cell walls have fine, spiral thickenings. Exodermal cells are thin-walled. The cortex features scattered thick-walled cells and in some cases branched bars of secondary cell wall material. Endodermis is either u-or O-thickened, but pericycle is always O-thickened opposite the phloem. Vascular tissue consists of alternating strands of xylem and phloem surrounded by a matrix of thick-walled cells. Pith cells may be parenchymatous or sclerenchymatous.     

STUDIES ON THE FLORAL ANATOMY OF THE CUNONIACEAE

Twenty-two genera representing sixty-two species of Cunoniaceae and Davidsonia were examined with respect to floral anatomy. Sepals are vascularized by three traces with the lateral traces of adjacent sepals united. Pancheria is unique for the family with species in which the sepals are vascularized by a single, undivided bundle. Petals, when present, and stamens, are uniformly one-trace structures. A general tendency exists within the family for the principal floral bundles to unite in various ways, with fusions evident between calyx, corolla, and androecial vascular supplies. Carpel number ranges from two to five and the gynoecium is generally surrounded by a prominent disc. Gynoecia of Ceratopetalum and Pullea are “half-inferior.” The number of ovules per carpel locule ranges from one to numerous. Ventral carpel sutures range from open to completely sealed at the level of placentation. Carpels of the apocarpous genus Spiraeanthemum (incl. Acsmithia) are vascularized by a dorsal bundle and either three or four bundles constituting the ovular and wing vasculation in the ventral position, a condition unlike other members of the family. Ovules are supplied by the median ventral bundle. More advanced bicarpellate gynoecia within the family are predominately vascularized by a dorsal and two ventral bundles although a variable number of additional lateral wall traces may be present. A major trend exists toward fusion of the ventral bundles of adjacent carpels in the ovary of both bicarpellate and multicarpellate plants. At the base of the styles the fused ventral strands separate and extend along with the dorsal carpellary bundles into styles of adjacent carpels. In Pullea the ventral bundles terminate within the ovules. The united ventral carpellary bundles in Aphanopetalum, Gillbeea, and Aistopetalum lie in the plane of the septa separating adjacent carpels. Ovules are vascularized by traces originating from the vascular cylinder at the base of the gynoecium or by traces branching from the ventral bundles. Ovular traces in each carpel are united, or remain as discrete bundles, prior to entering the placenta. Tannin and druses are common throughout all floral parts. Although floral anatomy generally supports the position of Cunoniaceae near Saxifragaceae and Davidsoniaceae, the evolutionary relationship of the Cunoniaceae to the Dilleniaceae is uncertain.     

COMPARATIVE ANATOMY OF THE PETIOLE AND INFRAGENERIC RELATIONSHIPS IN JATROPHA (EUPHORBIACEAE)

Anatomical features of the petiole in several species of Jatropha L. (Euphorbiaceae) are presented as evidence in support of infrageneric relationships. A trilacunar 3-trace nodal pattern is typical for the genus. The vascular supply to the stipules is derived from the branching of the two peripheral leaf traces. The number of vascular bundles range from 11 through 9, 7, 5 and 3, and occur in a ring, as free traces, a medullated cylinder, or as U-shaped free traces. The reduction from nine to three bundles is correlated with the gross morphological features while 11, which occurs only in the section Peltatae (Pax) Dehgan & Webster, presents an increase. Reduction in the number of petiolar traces follows the evolutionary advancement of various taxa. This reduction in traces corresponds with south-north distribution of the species and consequential adaptation to colder and more arid climates in Central America and Africa. Smaller leaves, fewer primary veins and fewer vascular traces have resulted as a response to reduced need for water. Presence of dorsal (super-numerary) bundles which supply the petiolar glands in subgenus Jatropha (= Adenoropium Pax) is considered significant, since African taxa of the section (subsection Pubescentes Pax) have retained these bundles despite the loss of petiolar glands. The latter glands are prominent in the South American and Indian species. Sectional lines in the genus can, therefore, be drawn generally on the basis of numerical constancy and relative uniformity in the arrangement of petiolar traces. The continuity of vascular bundles from the stem into the petiole and variations of bundle arrangements are depicted in three-dimensional drawings.     

The composition and timing of flower odour emission by wild <Emphasis Type="Italic">Petunia axillaris</Emphasis> coincide with the antennal perception and nocturnal activity of the pollinator <Emphasis Type="Italic">Manduca sexta</Emphasis>

In the genus Petunia, distinct pollination syndromes may have evolved in association with bee-visitation (P. integrifolia spp.) or hawk moth-visitation (P. axillaris spp). We investigated the extent of congruence between floral fragrance and olfactory perception of the hawk moth Manduca sexta. Hawk moth pollinated P. axillaris releases high levels of several compounds compared to the bee-pollinated P. integrifolia that releases benzaldehyde almost exclusively. The three dominating compounds in P. axillaris were benzaldehyde, benzyl alcohol and methyl benzoate. In P. axillaris, benzenoids showed a circadian rhythm with an emission peak at night, which was absent from P. integrifolia. These characters were highly conserved among different P. axillaris subspecies and P. axillaris accessions, with some differences in fragrance composition. Electroantennogram (EAG) recordings using flower-blends of different wild Petunia species on female M. sexta antennae showed that P. axillaris odours elicited stronger responses than P. integrifolia odours. EAG responses were highest to the three dominating compounds in the P. axillaris flower odours. Further, EAG responses to odour-samples collected from P. axillaris flowers confirmed that odours collected at night evoked stronger responses from M. sexta than odours collected during the day. These results show that timing of odour emissions by P. axillaris is in tune with nocturnal hawk moth activity and that flower-volatile composition is adapted to the antennal perception of these pollinators.     

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.     

DEVELOPMENTAL ANATOMY OF THE STEM OF WELFIA GEORGII,IRIARTEA GIGANTEA,AND OTHER ARBORESCENT PALMS: IMPLICATIONS FOR MECHANICAL SUPPORT

Changes in stem anatomy with radial position and height were studied for the arborescent palms Welfia georgii, Iriartea gigantea, Socratea durissima, Euterpe macrospadix, Prestoea decurrens, and Cryosophila albida. Vascular bundles are concentrated toward the stem periphery and peripheral bundles contain more fibers than central bundles. Expansion and cell wall thickening of fibers within vascular bundles continues throughout the life of a palm, even in the oldest tissue. Within individual vascular bundles, the fibers nearest the phloem expand first and fiber cell walls become heavily thickened. A front of expanding fibers moves outward from the phloem until all fibers within a vascular bundle are fully expanded and have thick cell walls. Peripheral vascular bundles differentiate first and inner bundles later. In the stem beneath the crown, vascular bundles and ground tissue cells show little or no size increase, but marked cell wall thickening during development for Welfia georgii. Beneath the crown, diameters of peripheral vascular bundles increase more than twofold for Iriartea gigantea, while diameters of central bundles do not increase. In Iriartea stems, ground tissue cells at the periphery elongate to accommodate expanding vascular bundles and cell walls become thickened to a lesser degree than in fibers; central ground tissue cells elongate markedly, but cell walls do not become thickened; and large lacunae form between central parenchyma cells. For Iriartea, Socratea, and Euterpe, sustained cell expansion results in limited, but significant increases in stem diameter. For all species, sustained cell wall thickening results in dramatic increases in stem stiffness and strength.     

The primary vascular system of Callixylon

The primary vascular system of Callixylon (main stem axes of Archaeopteris) is composed of a discontinous cylinder of longitudinal bundles from some of which traces diverge radially in a regular, helical pattern. Tangential divisions and fusions of primary xylem strands occur in approximately equal frequency and, thus, the number of bundles in the system remains constant in the specimen studied. Following divergence, traces increase in size and become ribbed distally. The available evidence suggests that all of the traces observed in this study are branch traces. Branch bases, embedded in secondary xylem, have the anatomical characteristics of penultimate axes of lateral branch systems of Archaeopteris. It is suggested that some regions of main axes of Archaeopteris might have borne lateral branch systems only, lacking entirely simple leaves. Lateral branch systems, therefore, might have been more similar to compound leaves than previously supposed.     

Nuove Stazioni di Festuca Laxa Host in Territorio Italiano e Considerazioni Sistematiche Sulla Sua Indipendenza Da Festuca Dimorpha Guss

Abstract

New localities of «Festuca laxa» Host in the Italian territory and systematic considerations about its indipendence from «F. dimorpha» Guss. Some new localities of Festuca laxa are given for the Alps of Friuli (Northeastern Italy), which show that this species takes part also of Italian Flora. Until now it was known only for Austria and Jugoslavia. The paper furthermore deals with some anatomical differences in the leaf — structure of the two fescues, as to see in transections. F. laxa has normally 3 larger vascular bundles, which are wholly enclosed by T-shaped sclerenchyma and 4(8–9) smaller veins, where the sclerenchyma occurs only in the abaxial face of the blade. F. dimorpha on the contrary has 5 larger bundles and usually 6 smaller ones. The number of the secondary veins depends in both cases on the various sizes of the leaves. Also the cenotic and ecological behaviour of F. laxa is shortly illustrated on the basis of two phytosociological records.     

COMPARATIVE ANATOMY OF THE SEED COATS OF GNETUM AND THEIR PROBABLE EVOLUTION

The seed coats of Gnetum gnemon L., G. ula Brongn., G. montanum f. parvifolium (Warb.) Mgf. and G. neglectum Bl. consist of three layers. The outer layer or sarcotesta is mostly parenchyma but contains some sclereids and fibers and a series of simple vascular bundles. The middle sclerotesta forms masses of sclereids in varying shapes and numbers, sometimes extending as a basal plate, and is usually thicker near the micropylar tube. The second layer also contains a series of small vascular bundles that reach the apex. Depending on the species, the middle layer is sometimes nearly free from the outer layer, may be partially fused with it, or completely fused to it at maturity. The innermost layer of the seed coat constitutes the endotesta which is membranous and only rarely contains sclerenchyma. It possesses a dichotomous venation system with varying degrees of anastomosing, depending upon the species. The above species show qualitative and quantitative differences in their sclerenchyma and laticifers. Seed coat anatomy may be useful in the diagnosis of some species. The trends of evolution of seed coat structure within these four species of Gnetum are discussed, and a comparison of tissue layers and vasculature with certain fossil pteridosperms is made, especially in the Trigonocarpales