Guaiacyl Lignin Associated with Vessels in Aspen Callus Cultures

Lignin from aspen (Populus tremuloides Michx.) tissue cultures containing only mature vessels and undifferentiated parenchymatous cells is exclusively of the guaiacyl type normally associated with gymnosperms. This supports the theory that the guaiacyl and syringyl lignin in angiosperm wood is compartmentalized, with guaiacyl lignin in vessels and syringyl lignin in fibers and ray cells.     

Water-storing and Cavitation-preventing Adaptations in Wood of Cacti

Ancestral cacti presumably had abundant, fibrous, heavily lignifiedwood, similar to that present in the relictual, leaf-bearinggenus Pereskia. During the evolutionary radiation of the subfamilyCactoideae, diverse types of bodies and woods arose. Severalevolutionary lines have retained an abundant, fibrous wood:all wood cells, even ray cells, have thick lignified walls,and axial parenchyma is only scanty paratracheal. Aside froma diversity of vessel diameters, there seems to be little protectionagainst cavitation during water-stress, and little water-storagecapacity. This strong wood permits the plants to be tall andto compete for light in their tree-shaded semi-arid habitats.In other evolutionary lines, the wood lacks fibres, and almostall cells have thin, unlignified walls. Vessels occur in anextensive matrix of water-storing parenchyma, and tracheidsare also abundant, constituting over half the axial tissue insome species. There is excellent protection against cavitation,but little mechanical support for the plant body; however, theseplants are short and occur in extremely arid, unshaded sites.Scandent, vinelike plants of two genera produce a dimorphicwood—while their shoots are extending without externalsupport, they produce fibrous, lignified wood, but after leaningagainst a host branch, they produce a parenchymatous, unlignifiedwood.Copyright 1993, 1999 Academic Press Cactaceae, cactus, water-stress, wood, evolution, xylem     

Wide-band tracheids are present in almost all species of Cactaceae

Wide-band tracheids (WBTs) have been found in seedlings of most species of cacti that have fibrous wood in their adult bodies. Consequently, this cell type is now known to be present in almost all cacti. Earlier studies of adult plants revealed WBTs to be present only in cacti with globose or short, broad bodies, whereas all species with large columnar or long slender bodies had fibrous wood without WBTs. However, even these species produce WBTs during the first several months after germination. In species with fibrous wood in their adult bodies (species with large or slender bodies), seedlings undergo a phase transition in wood morphogenesis after a few months and stop producing the juvenile (WBT) wood and begin producing adult (fibrous) wood. If adult plants have an intermediate size, the phase transition is delayed and the plant produces WBT wood for several years. Species with globose bodies repress the phase transition completely and never switch to producing adult (fibrous) wood. Because WBTs are so widespread, they probably originated only once in Cactaceae, not multiple times as suggested earlier, or there may have been just a single origin in the Cactaceae/Portulacaceae clade.     

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.     

Systematic and phylogenetic value of wood anatomy in Heteromorpheae (Apiaceae,Apioideae)

The wood anatomy of all four woody genera of the tribe Heteromorpheae (Apiaceae, subfamily Apioideae) has been described and compared, based on 40 wood samples (representing nine species of Anginon, one species of Glia, three species of Heteromorpha and two species of Polemannia). The four genera were found to be relatively similar in their wood anatomy. Helical thickenings on the vessel walls occur in all species investigated and appear to represent an ancestral character state and a symplesiomorphy for the tribes Bupleurieae and Heteromorpheae. Each of four genera has a diagnostically different combination of character states relating to the diameter of vessels, size of intervessel pits, length of fibres, presence and arrangement of banded axial parenchyma, size of rays and ray cells, and presence of septate fibres and crystals in the ray cells. The occurrence of marginal axial parenchyma in Anginon and Glia may be an additional synapomorphy for these taxa. Variation in the wood anatomy of 31 samples from nine species of Anginon is not correlated with habitat (Fynbos or Succulent Karoo Biomes), but instead appears to reflect adaptations to seasonal aridity found in both ecosystems. © 2008 The Linnean Society of London, Botanical Journal of the Linnean Society, 2008, 158 , 569–583.     

WOOD FORMATION IN PROSOPIS: EFFECT OF 2,4-D, 2,4,5-T,AND TIBA

Treatment of erect stems of Prosopis with near phytotoxic levels of 2,4-D or 2,4,5-T causes the formation of an unusual wood with narrow, thick-walled vessels and axial parenchyma in which cell wall thickening is inhibited. Although reduced in diameter, the vessels formed during 2,4-D and 2,4,5-T treatment are so numerous that there is no significant difference between phenoxyacetic acid and control seedling groups with regard to total area of xylem occupied by vessels. The preferential maturation of xylem vessels over parenchyma and the transformation of fusiform initials into septate parenchyma strands in phenoxyacetic acid-treated Prosopis resemble the structural changes reported to occur after girdling in the cambial tissue of other arborescent angiosperms. Bending experiments indicate that tension-wood fibers of Prosopis differentiate in response to an auxin deficiency. However, xylogenesis in erect stems treated with TIBA is affected such that a significantly higher proportion of the cambial cell population becomes axial xylem parenchyma.     

Wood and bark anatomy of Muntingiaceae: A phylogenetic comparison within Malvales s. l.

Quantitative and qualitative data on wood and bark anatomy are given for Muntingia calabura L. and Dicraspidia donnell-smithii Standley. These data are compared with phylogenetic schemes, based on DNA analysis, in which Muntingiaceae belong to the “dipterocarp clade” within Malvales. The data are consistent with this hypothesis, although Muntingiaceae lack pit vestures in vessels, which are seen in the other malvalean families (Cistaceae, Dipterocarpaceae, Neuradaceae, Sarcolaenaceae, Thymeleaceae), and this may represent a loss of pit vestures. All families of the dipterocarp clade agree with both genera of Muntingiaceae in having tracheids as the imperforate tracheary element type (at least ancestrally), although fiber-tracheids also occur in some Dipterocarpaceae and Thymeleaceae. The large size of some malvalean families (with attendant greater diversity in character states) and a paucity of wood studies in those families make for difficulty in comparison of features such as axial parenchyma and ray types with those of Muntingiaceae; character states of these features are consistent with placement of Muntingiaceae in the dipterocarp clade of Malvales. Banded phloem fibers in bark of Muntingiaceae are much like those of other Malvales. Wood of Muntingiaceae is highly mesomorphic according to quantitative vessel features.     

Evolution of extreme xeromorphic characters in wood: a study of nine evolutionary lines in Cactaceae

Vessels of xeric-adapted woods have been predicted to be narrower than those of mesic-adapted woods, to occur at higher densities, to occur in larger clusters, and to have a greater percentage of them in clusters. These predictions were tested by comparing wood structure of several evolutionary lines of xeric-adapted cacti to that of mesic-adapted Pereskia, which probably resembles the ancestral cacti. Although derived cacti occur in habitats with water stress ranging from mild (rain forests) to severe (open deserts with little vegetation other than cacti), as long as plants retain wood with an ordinary fibrous matrix, wood characters are remarkably uniform and not correlated with habitat aridity. However, in several evolutionary lines, novel wood types occur with characters that fulfill the predictions for xeric-adapted woods listed above. However, conductive area (fraction of wood transverse-sectional area occupied by conduits) and estimated specific conductance (conductance per square millimetre) are correlated with shoot height (the need for mechanical support from xylary fibers) rather than with habitat aridity: tall plants transport water through relatively few, wide vessels, permitting much of the wood volume to consist of fibers. Small plants with little wood use large numbers of narrow vessels rather than small numbers of wide ones, thereby achieving conductive safety.     

KLEINODENDRON AND XYLEM ANATOMY OF CLUYTIEAE (EUPHORBIACEAE)

Kleinodendron, a new genus of Euphorbiaceae, was assigned by Smith and Downs to the tribe Cluytieae. A xylem anatomical survey indicates that there are no objections to this placement. Woods of Cluytieae are diverse but may be characterized generally by having pores which average less than 80 μ in diameter and which are well divided between solitary and radial multiple distributions in the same species; simple vessel perforations; alternate intervascular pitting; fiber-tracheids and libriform wood fibers; exclusively uniseriate, or uniseriate and biseriate heterocellular vascular rays in the same species; uniseriate “bridges” linking superposed biseriate ray segments; diffuse, diffuse-in-aggregates, and scanty vasicentric axial parenchyma, sometimes in the same species; and crystal rhomboids. That Microdesmis and Pogonophora diverge sharply from these generalizations in having scalariform vessel perforations and broad vascular rays, is an indication that they may not be closely related to other genera in Cluytieae.     

Wood specific gravity and anatomy in Heliocarpus appendiculatus (Tiliaceae)

Specific gravity exhibits extremely large radial increases with distance from the pith in Heliocarpus appendiculatus Turcz. (Tiliaceae), a pioneer of neotropical wet forests. To determine some of the wood anatomical changes associated with this increase, wood samples taken at breast height from three trees were divided into 1.0-cm-long segments from pith to bark. Measurements were made of fiber wall thickness, fiber lumen diameter, and percentages of fibers, axial parenchyma, ray parenchyma, and vessels on sections prepared from each segment. The extreme radial increases in specific gravity were associated with increases in fiber wall thickness, decreases in fiber diameter, decreases in fiber lumen diameter, and changes in the relative proportions of fibers and parenchyma. The increase in percent fiber concomitant with a decrease in axial parenchyma was the most important contributor to the increase in specific gravity in this species. The best predictor of specific gravity was percent fibers (r = 0.91, 0.92, 0.94) or percent axial parenchyma (r = -0.92, -0.91, -0.95), two variables that were highly intercorrelated (r = -0.95, -0.98, -0.99).     

Successive cambia in Aizoaceae: products and process

The transverse and longitudinal sections of the stems and roots of 11 genera of Aizoaceae, representing a wide range of growth forms from hard fibrous stems to fibre‐free roots, were studied using light microscopy and scanning electron microscopy. In most of the genera, fibres are the first xylary product of each vascular cambium, followed by vessels in a parenchyma background. Variations on this pattern help to prove that fibres are produced by vascular cambia, except in Ruschia and Stayneria, in which both the lateral meristem and the vascular cambia produce fibres. Cylinders of conjunctive tissue parenchyma that alternate with the vascular cylinders are produced by the lateral meristem. The concept that the lateral meristem gives rise to the vascular cambia and secondary cortex is supported by photographic evidence. Radial divisions occur in the origin of the lateral meristem, and then again as vascular cambia arise from the lateral meristem; these radial divisions account for storeying in fibres and conjunctive tissue. Raylessness characterizes all Aizoaceae studied, with the exception of Tetragonia, which also differs from the remaining genera by having vasicentric axial parenchyma, a scattering of vessels amongst fibres, and the presence of druses instead of raphides. Several vascular cambia are typically formed per year. Several vascular cambia are active simultaneously in a given stem or root. Roots have fewer fibres and more abundant conjunctive tissue parenchyma than stems. Successive cambia result in an ideal dispersion of vascular tissue with respect to water and photosynthate storage and retrieval capabilities of the parenchyma, and to liana stem plans. The distribution and relative abundance of fibres, vessels, secondary phloem, and conjunctive tissue parenchyma relate primarily to habit and are not a good source of systematic data, with the probable exception of Tetragonia. The general pattern of lateral meristem and vascular cambial ontogeny is the same as in other families of the core Caryophyllales, although the patterns of the tissues produced are diverse. © 2007 The Linnean Society of London, Botanical Journal of the Linnean Society, 2007, 153 , 141–155.     

Chemical Composition of Cacti Wood and Comparison with the Wood of Other Taxonomic Groups

The aims of this study were to determine the wood chemical composition of 25 species of Cactaceae and to relate the composition to their anatomical diversity. The hypothesis was that wood chemical components differ in relationship to their wood features. The results showed significant differences in wood chemical compounds across species and genera (P < 0.05). Pereskia had the highest percentage of lignin, whereas species of Coryphantha had the lowest; extractive compounds in water were highest for Echinocereus, Mammillaria, and Opuntia. Principal component analysis showed that lignin proportion separated the fibrous, dimorphic, and non‐fibrous groups; additionally, the differences within each type of wood occurred because of the lignification of the vascular tissue and the type of wall thickening. Compared with other groups of species, the Cactaceae species with fibrous and dimorphic wood had a higher lignin percentage than did gymnosperms and Acer species. Lignin may confer special rigidity to tracheary elements to withstand desiccation without damage during adverse climatic conditions.     

WOOD ANATOMY AND RELATIONSHIPS OF LACTORIDACEAE

Mature wood of Lactoris, not previously available for study, reveals ten distinctive characters: vessels with simple perforation plates; vessels in pore multiples; vessel-to-axial parenchyma pits scalariform or transitional, vessel-to-vessel pits alternate; fiber-tracheids with vestigial pits; fiber-tracheids, vessels, and axial parenchyma storied; axial parenchyma vasicentric scanty; axial parenchyma either not subdivided or, if subdivided, with thin nonlignified walls between the cells (like the septa in septate fibers); rays wide and tall, little altered during ontogeny; ray cells upright; and ray cells taller adjacent to fascicular areas. All of these features occur in woods of Piper and other Piperaceae. The systematic position of Lactoris is therefore reassessed. Evidence available to date is consonant with placement of Lactoridaceae in Piperales, in which it would be more primitive than Piperaceae or Saururaceae. Features cited as evidence for alternative placements of Lactoridaceae are reviewed.     

Asteropeia and Physena (Caryophyllales): A case study in comparative wood anatomy

Previous analyses ofAsteropeia andPhysena have not compared the wood anatomy of these genera to those of Caryophyllales s.l. Molecular evidence shows that the two genera from a clade that is a sister group of the core Caryophyllales. Synapomorphies of theAsteropeia-Physena clade include small circular alternate pits on vessels, presence of vasicentric tracheids plus fiber-tracheids, presence of abaxial-confluent plus diffuse axial parenchyma, and presence of predominantly uniseriate rays. These features are analyzed with respect to habit and ecology of the two genera. Solitary vessels, present in both genera, are related to the presence of vasicentric tracheids. Autapomorphies in the two genera seem related to adaptations byPhysena as a shrub of moderately dry habitats (e.g., narrower vessel elements, abundant vasicentric tracheids, square to erect cells in rays) as compared to alternate character expressions that seem related to the arboreal habit and humid forest ecology ofAsteropeia. The functional significance of vasicentric tracheids and fiber-tracheids in dicotyledons is briefly reviewed in the light of wood anatomy of the two genera.     

Ontogenetic mechanisms and the evolution of Cactaceae

Abstract

The ancestors of cacti were leafy trees that had hard, woody trunks. The development of the cactus body is controlled by ontogenetic mechanisms that have evolved, and now they produce a body that is leafless, succulent and has a photosynthetic cortex. Specific changes include: bark formation is postponed and the epidermis and stomata function for many years; the outer cortex is a palisade cortex with intercellular spaces; there are cortical bundles that resemble leaf veins but which have secondary xylem and phloem. Wood development has changed dramatically such that water storage is maximized (increased ray parenchyma) and danger of water stress is minimized (increased paratracheal parenchyma, loss of fibers). Several genera have polymorphic wood: the plants produce one type of wood for several years, then later they produce a different type. It is possible that the extensive evolutionary changes have resulted from mutations in the controller regions of genes, not in the structural regions.     

Contributions to the Wood Anatomy of the Rubioideae (Rubiaceae)

Damnacanthus , Lasianthus, Saldinia, and Trichostachys are also included. Wood anatomical characters are compared with recent phylogenetic insights into the study group on the basis of molecular data. The observations demonstrate that the delimitation and separation of several taxa from the former Coussareeae/Morindeae/Prismatomerideae/Psychotrieae aggregate is supported by wood anatomical data. The Coussareeae can be distinguished from the other Rubioideae by their scanty parenchyma, septate libriform fibres, and the combination of uniseriate and very high multiseriate rays with sheath cells. Axial parenchyma bands and fibre-tracheids characterise Gynochtodes and some species of Morinda (Morindeae s.str.), but the latter genus is variable with respect to several features (e.g. vessel groupings and axial parenchyma distribution). Wood data support separation of Rennellia and Prismatomeris from Morindeae s.str.; vessels in both genera are exclusively solitary and axial parenchyma is always diffuse to diffuse-in-aggregates. Damnacanthus differs from the Morindeae alliance by the occurrence of septate fibres, absence of axial parenchyma, and the occasional presence of fibre wall thickenings. There are interesting similarities between members of the Lasianthus clade and the Pauridiantheae/Urophyleae group such as the sporadic occurrence of spiral thickenings in axial parenchyma cells. Received 26 January 2001/ Accepted in revised form 6 June 2001     

Wood anatomy of Gentianaceae, tribe Helieae, in relation to ecology, habit, systematics, and sample diameter

Twenty collections representing one species each ofSymbolanthus andTachia, and 17 species ofMacrocarpaea were studied by means of light microscopy and scanning electron microscopy (SEM). Wood details show that the three genera form a coherent group;Tachia differs from the others in only a few minor characters. Because the species studied form a natural group, wood variations within Helieae offer the basis for correlations and interpretations with respect to habit and ecology. Diameter of stems studied proves to be an important variable that must be taken into account. Correlations with stem diameter include wider vessels in outer wood of wider samples. This would correspond to deeper penetration of reliable water tables by roots of helioid trees or large shrubs. Ray height decreases with increase in stem diameter, an indication of paedomorphosis. Rays of all species are paedomorphic in histology by virtue of relative paucity or even absence of procumbent cells in multiseriate rays. Pseusoscalariform lateral wall pitting of vessels is also a feature characteristic of paedomorphosis. The assemblage of paedomorphic features correlates well with the conclusion, reached by authors who used cladistic methods, that Gentianaceae other than Gentianeae are derived from suffrutescent prennials. The Mesomorphy Ratio, which incorporates three vessel features, correlates with leaf length and with stem diameter. All Helieae are mesophytic, but to various degrees. Septate fiber-tracheids, where present, are typically near vessels and form a substitute for or an addendum to vasicentric axial parenchyma as a mechanism for photosynthate storage. Vestured pits occur on lateral wall pits of vessels of all Helieae, but not on the fibertracheids. Vestured pits show diversity withinMacrocarpaea, a feature of possible systematic significance.     

EVOLUTION OF POLYSPORANGIATE ANTHERS IN ONAGRACEAE

The microsporogenous tissue of at least some species of all 17 genera of Onagraceae is divided by transverse septa composed only of tapetum or of both tapetum and parenchyma. The presence of these septa apparently constitutes a distinctive characteristic of the family. In Calylophus sect. Salpingia, Gaura, Clarkia, Heterogaura, and two unrelated species of Ludwigia, the septa are transverse and mostly parenchymatous. In Hauya and Calylophus sect. Calylophus, similar transverse septa together with vertical ones divide the sporogenous tissue into many small spheroidal or ellipsoidal packets. The condition in which occasional tapetal septa divide the sporogenous tissue is clearly the ancestral one in Onagraceae. Polysporangiate anthers divided by parenchymatous septa have evolved independently at least twice each in the branches leading to Ludwigia and to all other members of the family, for a total of no less than four times. Based on this feature and the unique pattern of histogenesis of their integuments, Hauya (despite its retention of many plesiomorphic features), Calylophus, and Gaura may well be directly related to one another.     

Vessel elements present in the secondary xylem of Trochodendron and Tetracentron (Trochodendraceae)

For almost 150 years, the two monotypic genera Trochodendron and Tetracentron (Trochodendraceae) have been considered to share an unusual and primitive feature in angiosperms - the lack of vessels in their wood. Therefore, they have been classified in a basal position in the angiosperms. Our observations by light microscopy, low-vacuum environmental scanning electron microscopy (ESEM) and high-vacuum scanning electron microscopy (SEM) both in fresh and FAA-fixed materials consistently showed the presence of tracheary elements differentiated into two types in both genera. In Trochodendron, the tracheary elements can be divided into perforate vessel elements and imperforate fiber-tracheids and tracheids. The vessel elements show end and lateral walls. The pits on the end walls are elongate- broadened and do not have membranes or only a few remnants of them forming the perforation plates. The fiber-tracheids show crossfield pit pairs and sharp ends, and the tracheids show bordered pits. In Tetracentron, the tracheary elements comprise vessel elements and fibers. The vessel elements are similar to those of Trochodendron, whereas the fibers have no crossfield pit pairs but, rather, elliptical pits and sharp ends. Thus, both Trochodendron and Tetracentron are vessel bearing rather than vesselless, although their vessel elements are primitive.