The fossil record of Cunoniaceae: new evidence from Late Cretaceous wood of Antarctica?

Fossil angiosperm wood from Upper Cretaceous sediments of Livingston Island and James Ross Island in the northern Antarctic Peninsula region is identified as having the combination of anatomical characters most similar to modern Cunoniaceae. The material is characterised by predominantly solitary vessels, opposite to scalariform intervessel pitting, scalariform perforation plates, heterocellular multiseriate and homocellular uniseriate rays, diffuse axial parenchyma. Anatomically, the specimens conform most closely to the fossil organ genus Weinmannioxylon Petriella which has been placed within the Cunoniaceae. The presence of Weinmannioxylon in Late Cretaceous sediments suggests that taxa within or stem taxa to the Cunoniaceae might have been a notable component of the forest vegetation that covered the Antarctic Peninsula during the Late Mesozoic and may therefore represent the earliest record of this family.     

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.     

Observations on the vegetative anatomy of Austrobaileya: habital, organographic and phylogenetic conclusions

For the single species of Austmbaileya (Austrobaileyaceae), quantitative and qualitative data are offered on the basis of a mature stem and a root of moderate diameter. Data available hitherto have been based on stems of small to moderate diameter, and roots have not previously been studied. Scanning electron microscope (SEM) photographs are utilized for roots, and show compound starch grains. Roots lack sclerenchyma but have relatively narrow vessels and abundant ray tissue. Recent phylogenies group Austrobaileyaceae with the woody families Illiciaceae, Schisandraceae, and Trimeniaceae (these four may be considered Illiciales), and somewhat less closely with the vesselless families Amborellaceae and Winteraceae and the aquatic families Cambombaceae and Nymphaeaceae. The vessel-bearing woody families above share vessels with scalariform perforation plates; bordered bars on plates; pit membrane remnants present in perforations; lateral wall pitting of vessels mostly alternate and opposite; tracheids and/or septate fibre-tracheids present; axial parenchyma vasicentric (sometimes abaxial); rays Heterogeneous Type I; ethereal oil cells present; stomata paracytic or variants of paracytic. Although comparisons between vessel-bearing and vesselless families must depend on fewer features, Amborellaceae and Winteraceae have no features incompatible with their inclusion in an expanded Illiciales.     

Distribution of scalariform and simple perforation plates within the vessel network in secondary xylem of Araliaceae and its implications for wood evolution

The distribution of scalariform and simple perforation plates along vessels in Arthrophyllum otopyrenum, Meryta tenuifolia, and Polyscias multijuga (Araliaceae) is examined. In all three species, most vessels bear simple perforation plates only, but the combination of simple and scalariform perforation plates in variable ratios also occurs. Aggregated arrangement of scalariform perforation plates along the vessels was statistically confirmed in some vessel portions. The scalariform perforation plates occur mostly in narrow vessels that are grouped in multiples. Within the clade represented by Polyscias and Arthrophyllum, the evolutionary transition from scalariform to simple perforation plates is realized as the gradual elimination of vessels or vessel portions with scalariform perforation plates, but is not accompanied by a gradual decrease of the number of bars per perforation plate. The narrow vessels that are grouped in vessel multiples are likely to retain the ability to develop scalariform plates, which could promote the evolution from simple to scalariform perforation plates as is the case within Meryta.     

Wood anatomy of theSarraceniaceae; ecological and evolutionary implications

The wood of theSarraceniaceae has a considerable number of primitive features including scalariform perforation plates, long and oblique end walls, scalariform lateral wall pitting, solitary vessels, tracheids with scalariform pitting, and diffuse axial parenchyma. Vessel elements in the genusHeliamphora have the greatest number of primitive features, while vessel elements inDarlingtonia andSarracenia appear to have modifications relating to temperate climates. The wood anatomy suggests thatHeliamphora is growing in a habitat more similar to the original habitat for the family thanDarlingtonia andSarracenia. The wood of theSarraceniaceae is similar to the wood of theTheales.     

Stem anatomy of the dwarf subshrub Cressa cretica L. (Convolvulaceae)

Stem anatomy and development of medullary phloem are studied in the dwarf subshrub Cressa cretica L. (Convolvulaceae). The family Convolvulaceae is dominated by vines or woody climbers, which are characterized by the presence of successive cambia, medullary- and included phloem, internal cambium and presence of fibriform vessels. The main stems of the not winding C. cretica shows presence of medullary (internal) phloem, internal cambium and fibriform vessels, whereas successive cambia and included phloem are lacking. However, presence of fibriform vessels is an unique feature which so far has been reported only in climbing members of the family. Medullary phloem develops from peri-medullary cells after the initiation of secondary growth and completely occupies the pith region in fully grown mature plants. In young stems, the cortex is wide and formed of radial files of tightly packed small and large cells without intercellular air spaces. In thick stems, cortical cells become compressed due to the pressure developed by the radial expansion of secondary xylem, a feature actually common to halophytes. The stem diameter increases by the activity of a single ring of vascular cambium. The secondary xylem is composed of vessels (both wide and fibriform), fibres, axial parenchyma cells and uni-seriate rays. The secondary phloem consists of sieve elements, companion cells, axial and ray parenchyma cells. In consequence, Cressa shares anatomical characteristics of both climbing and non-climbing members. The structure of the secondary xylem is correlated with the habit and comparable with that of other climbing members of Convolvulaceae.     

Occurrence and specialization of vessels in Xyridales

The occurrence and variation among vessels in available parts of 41 species in 16 genera of Rapateaceae and of 20 species in the four genera of Xyridaceae were determined. The vessels in Xyridaceae are more specialized in all organs of the plant than they are in Rapateaceae. Simple and scalariform perforation plates occur in the inflorescence axes and leaves of nearly all species of Xyridaceae but only scalariform plates occur in these organs of Rapateaceae – infrequently vessels are lacking in stems and leaves, at least in early metaxylem. Vessels in roots and stems of Mono–tremeae are most specialized (simple and scalariform plates) among tribes of Rapateaceae, with those in Rapateeae intermediate, and those in Schoenocephalieae and Saxofridericieae most primitive (only scalariform perforation plates). Brief comments are made about vessels as possible indicators of relationships with other families.     

The development of the tuber in seedlings of five species of Dioscorea from Nigeria

Tubers in all five species develop from the hypocotyl region of the seedlingS. A perivascular cambium arises cutting off mainly starch-storing parenchyma and collateral vascular bundles to the inside. A phellogen gives rise to cork on the outside. Between the two cambial layers there may or may not be layers of parenchyma, not storing starch but containing raphides. The vascular bundles consist of xylem with vessels, scalariform tracheids and parenchyma; and phloem, with sieve tubes and parenchyma.     

Living Cells in Wood 3. Overview; Functional Anatomy of the Parenchyma Network

The very different evolutionary pathways of conifers and angiosperms are very informative precisely because their wood anatomy is so different. New information from anatomy, comparative wood physiology, and comparative ultrastructure can be combined to provide evidence for the role of axial and ray parenchyma in the two groups. Gnetales, which are essentially conifers with vessels, have evolved parallel to angiosperms and show us the value of multiseriate rays and axial parenchyma in a vessel-bearing wood. Gnetales also force us to re-examine optimum anatomical solutions to conduction in vesselless gymnosperms. Axial parenchyma in vessel-bearing woods has diversified to take prominent roles in storage of water and carbohydrates as well as maintenance of conduction in vessels. Axial parenchyma, along with other modifications, has superseded scalariform perforation plates as a safety mechanism and permitted angiosperms to succeed in more seasonal habitats. This diversification has required connection to rays, which have concomitantly become larger and more diverse, acting as pathways for photosynthate passage and storage. Modes of growth such as rapid flushing, vernal leafing-out, drought deciduousness and support of large leaf surfaces become possible, advantaging angiosperms over conifers in various ways. Prominent tracheid-ray pitting (conifers) and axial parenchyma/ray pitting to vessels (angiosperms) are evidence of release of photosynthates into conductive cells; in angiosperms, this system has permitted vessels to survive hydrologic stresses and function in more seasonal habitats. Flow in ray and axial parenchyma cells, suggested by greater length/width ratios of component cells, is confirmed by pitting on end walls of elongate cells: pits are greater in area, more densely placed, and are often bordered. Bordered pit areas and densities on living cells, like those on tracheids and vessels, represent maximal contact areas between cells while minimizing loss of wall strength. Storage cells in rays can be distinguished from flow cells by size and shape, by fewer and smaller pits and by contents. By lacking secondary walls, the entire surfaces of phloem ray and axial phloem parenchyma become conducting areas across which sugars can be translocated. The intercontinuous network of axial parenchyma and ray parenchyma in woods is confirmed; there are no “isolated” living cells in wood when three-dimensional studies are made. Water storage in living cells is reported anatomically and also in the form of percentile quantitative data which reveal degrees and kinds of succulence in angiosperm woods, and norms for “typically woody” species. The diversity in angiosperm axial and ray parenchyma is presented as a series of probable optimal solutions to diverse types of ecology, growth form, and physiology. The numerous homoplasies in these anatomical modes are seen as the informative results of natural experiments and should be considered as evidence along with experimental evidence. Elliptical shape of rays seems governed by mechanical considerations; unusually long (vertically) rays represent a tradeoff in favor of flexibility versus strength. Protracted juvenilism (paedomorphosis) features redirection of flow from horizontal to vertical by means of rays composed predominantly or wholly of upright cells, and the reasons for this anatomical strategy are sought. Protracted juvenilism, still little appreciated, occurs in a sizeable proportion of the world’s plants and is a major source of angiosperm diversification.     

First record of Cercidiphylloxylon (Cercidiphyllaceae) from the Palaeocene of Fushun,NE China

Abstract Cercidiphylloxylon spenceri (Brett) Pearson is described from the Lizigou Formation, Palaeocene in China. The growth rings are distinct; pores are diffuse, solitary, with somewhat angular outlines in cross section; vessel elements long with long scalariform perforation plates; intervessel pitting is opposite to scalariform; fiber‐tracheids are present; axial parenchyma is scarce; rays are mostly biseriate and heterogeneous. All wood characters of the fossil specimen fall into the range of those of extant Cercidiphyllum (Cercidiphyllaceae). The finding is one of the earliest fossil wood records of Cercidiphyllaceae.     

The first record of fossil Vitaceae wood from the Southern Hemisphere,a new combination for Vitaceoxylon ramunculiformis,and reappraisal of the fossil record of the grape family (Vitaceae) from the Cenozoic of Australia

Austrovideira dettmannaegen. & sp. nov. from the early Oligocene Capella Flora in central Queensland is the first fossil Vitaceae wood described from the Southern Hemisphere. A new combination, Stafylioxylon ramunculiformis (Poole & Wilkinson) Pace & Rozefelds for a Northern Hemisphere fossil wood is also proposed. Austrovideira and Stafylioxylon share with Vitaceoxylon secondary xylem with two diameter classes of vessels, wide vessels usually solitary, narrow vessels forming radial chains, very wide and tall rays, scanty paratracheal parenchyma and septate fibres. Austrovideira differs from Vitaceoxylon in having scalariform intervessel pits and homocellular rays composed exclusively of procumbent cells. This combination of features is seen in the Ampelocissus‐Vitis clade, and a clearly stratified phloem with fibre bands alternating with all other axial elements and phloem rays rapidly dilating towards the periderm is restricted to Parthenocissus and Vitis. Stafylioxylon shares with Austrovideira the presence of scalariform intervessel pits but it differs from that genus in both ray composition and bark anatomy, as it lacks a stratified phloem. These fossil wood genera demonstrate that the lianescent habit in the Vitaceae was established by the Eocene in the Northern Hemisphere and by the Oligocene in the Southern Hemisphere. The pollen and seed fossil record shows that the Vitaceae were in Australia by the Eocene and fossil seeds suggest that the family had radiated by this time. The Oligocene Capella flora with two seed taxa and fossil wood (Austrovideira) provides further evidence of an Australian radiation. The fossil evidence, suggests a significant Gondwanic history for the family.     

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.     

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     

First record of Cercidiphylloxylon(Cercidiphyllaceae)from the Palaeocene of Fushun,NE China

Cercidiphylloxylon spenceri(Brett)Pearson is described from the Lizigou Formation,Palaeocene in China.The growth rings are distinct; pores are diffuse,solitary,with somewhat angular outlines in cross section;vessel elements long with long scalariform perforation plates; intervessel pitting is opposite to scalariform; fibertracheids are present; axial parenchyma is scarce; rays are mostly biseriate and heterogeneous.All wood characters of the fossil specimen fall into the range of those of extant Cercidiphyllum(Cercidiphyllaceae).The finding is one of the earliest fossil wood records of Cercidiphyllaceae.     

Stem anatomy of Caryophyllaceae

The xylem and phloem of 88 Caryophyllaceae from subtropical and temperate regions mainly in Western Europe and the Canary Islands are described and analysed. They are compared with their taxonomic classification, and assigned to their ecological range. The xylem of different life forms (herbaceous plants, dwarf shrubs and shrubs) consists mainly of parenchyma and small vessels that are 20–50 μm in diameter in earlywood. They have simple perforations and pits are pseudosclariform and scalariform. The axial parenchyma is mostly pervasive or paratracheal, and the ray cells are exclusively upright or square. The anatomy of the subfamily Alsinoideae is homogeneous and characterised by the absence of libriform fibres, large rays, crystal druses and sclereids in the cortex. The subfamily Caryophylloideae is less homogeneous and mainly characterised by the presence of crystal druses on the xylem and phloem, as well as the presence of intra-annual fibre bands. The subfamily Paronychioideae is heterogeneous; included phloem is most characteristic. Ecological trends are clearly expressed by the age of plants and the average annual radial growth rates. Plants tend to grow older and slower at higher altitudes. The presence of intra-annual fibre bands in the xylem is characteristic of Caryophylloideae at lower altitudes. The study suggests that taxonomic and ecological classifications and large-scale ecological trend studies must be based on large and homogeneous datasets and well-defined anatomical features.     

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.     

Systematic and phylogenetic implications of the wood anatomy of six Neotropical genera of Primulaceae

Our main goals were to identify diagnostic characters at the species, genus, and subfamily levels, find anatomical features with potential for future morphological and molecular (combined) phylogenetic analyses, and to reconstruct the evolution of wood anatomical characters in two subfamilies of Primulaceae in a molecular phylogenetic framework. We investigated twenty-seven species from the woody Myrsinoideae (4 genera) and Theophrastoideae (2 genera) using scanning electron, light, and epifluorescence microscopy. Samples were prepared using standard protocols. Based on the wood anatomical characters, we were able to identify synapomorphies and to detect evolutionary trends of interest for the genera and subfamilies. Both subfamilies share the presence of diffuse porosity, simple perforation plates, septate fibres, and scanty paratracheal axial parenchyma. Theophrastoideae species have rays?>?10 cells wide and short (<?350 µm) vessel elements, and Myrsinoideae have breakdown areas in rays and longer vessel elements. Ardisia and Stylogyne have scalariform intervessel pits, Myrsine exhibit breakdown areas in rays, and two Cybianthus species from subgenus Weilgetia have distinguishing features (e.g., scalariform perforation plate in C. nemoralis and the absence of rays in C. densiflorus). Overall, when combining characters, we were able to segregate the Neotropical Primulaceae subfamilies and genera from each other and from the subfamily Maesoideae based on wood anatomy.     

WOOD ANATOMY OF ILLICIUM (ILLICIACEAE): PHYLOGENETIC,ECOLOGICAL, AND FUNCTIONAL INTERPRETATIONS

Quantitative and qualitative features are reported for 23 collections of ten species of Illicium, sole genus of Illiciaceae. Vessel elements are long, thin-walled, and angular; perforation plates are scalariform and range from long to moderately long; vessel-ray pitting is scalariform to opposite. Tracheids bear fully bordered pits. Axial parenchyma is sparse, abaxial to vessels with some diffuse cells also present. Rays are both multiseriate and uniseriate; the former are lacking near the pith in some species. No erect sheathing cells are present on multiseriate rays, and procumbent cells become more abundant as stems increase in size. Four species from montane subequatorial highlands lack growth rings and helical sculpture in vessels; the remainder of Illicium species have these features. Notably narrow vessels and large numbers of vessels per sq. mm characterize the temperate species from northern limits for the genus, I. anisatum, I. floridanum, and I. parviflorum. Greater vessel density offers redundancy and greater safety and is correlated with greater frost and possibly greater fluctuation in moisture availability. These two ecological features are probably also related to the narrow vessel diameter, which may retard entry of air embolisms (lowered air entry values) in accord with the physiological considerations of Slatyer. Reduction of number of bars per perforation plate within Illicium is also correlated with the more northerly climates. An additional hypothesis for evolution of shorter vessel elements in dicotyledons is introduced: if, as claimed by Slatyer, air embolisms in vessels tend to stop at ends of vessel elements and thus do not disable entire vessels, shorter vessel elements would maximally localize air embolisms. Presence of helical sculpture and other forms of relief within vessels has been difficult to explain in conifers and dicotyledons; such features might help resist cavitations by increasing adhesion of water molecules to cell walls (hydration).     

Comparative palynological and wood anatomical studies of Indian Taxus wallichiana Zucc., Cephalotaxus mannii Hook. and Cephalotaxus griffithii Hook.

A comparative study of Taxus wallichiana Zucc., Cephalotaxus mannii Hook. and Cephalotaxus griffithii Hook. of two families Taxaceae and Cephalotaxaceae has been carried out in detail to support the taxonomic existence of two families. The comparative studies have been carried out on the basis of wood anatomy and palynology. The anatomical properties of wood including the tracheids, ray parenchyma, axial parenchyma and number of cross-field pits have been described in detail. The palynological studies include the shape, size and ultrastructure of pollen grains. These studies give a taxonomic support for the recognition of two different genera of families Taxaceae and Cephalotaxaceae which are closely related.     

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.