Ultrastructure and development of the gametophyte vaginula-sporophyte foot complex in the liverwort Targionia hypophylla L.

The development of the placental complex including the gametophyte vaginula and the bulbous foot of the sporophyte in the liverwort Targionia hypophylla L. (Marchantiales) was studied by transmission electron microscopy. The vaginula and foot are separated by an intervening space and each consist of parenchymatous cells without intercellular spaces. Transfer cells begin to differentiate at the gametophyte-sporophyte interface just prior the onset of meiosis. While a single epidermal transfer-cell layer has developed in the foot by the end of meiosis, a multilayered pattern of transfer cells is formed in the vaginula. Gametophyte transfer cells have wall labyrinths which decrease in complexity with distance from the foot, lack plasmodesmata, and show signs of degeneration in the proximity of the foot. During meiosis, amyloplasts of both vaginula and foot lack starch and develop some thylakoid grana. In the subsequent stage of spore maturation, obliteration of the wall labyrinth occurs in both gametophyte and sporophyte transfer cells. The developmental pattern of the placental complex in Targionia is discussed in relation to that of mosses.     

The sporophyte-gametophyte junction in the moss Acaulon muticum (Pottiaceae): EARLY STAGES OF DEVELOPMENT

The sporophyte-gametophyte junction in Acaulon muticum is composed of the sporophyte foot, the surrounding gametophyte vaginula, and an intervening placental space. At an early stage of development the foot has a large basal cell, characterized by extensive wall ingrowths beginning at the lowermost tip of the basal cell and extending along its tangential walls. Sporophyte cells in contact with the basal cell develop ingrowths on their outer tangential walls and on radial walls in contact with the basal cell. All sporophyte cells at this stage are characterized by numerous mitochondria, strands of endoplasmic reticulum, and dictyosomes, particularly in the cytoplasm adjacent to areas of extensive wall development. Plastids typically contain abundant starch reserves. As development proceeds, wall ingrowths become more extensive on all walls in the sporophyte foot but are never found on the upper wall of the basal cell in contact with the remainder of the sporophyte. Plastids in the foot contain fewer starch reserves later in development. Wall ingrowths are not visible in the cells of the gametophyte vaginula until well after extensive development has occurred in the sporophyte foot. Stacks or layers of endoplasmic reticulum are characteristic of the cells of the gametophyte vaginula, along with numerous mitochondria, dictyosomes, and well-developed plastids. Starch reserves typically are less abundant in cells of the gametophyte. The early development of extensive wall elaborations in the cells of the sporophyte foot, and particularly in the basal cell, may favor the rapid movement of water and nutrients from the gametophyte into the sporophyte at a time when rapid development in this minute, ephemeral moss is critical.     

Comparative development of the sporophyte–gametophyte junction in six moss species

Developmental anatomy of the sporophyte–gametophyte junction in six moss species is described with special reference to sporophyte penetration into the gametophytic tissue. The sporophyte–gametophyte junction in mosses is classified into two types based on vaginula morphology: in the “true vaginula” type, the junction involves only an epigonium derived from the archegonium, and in the other “shoot vaginula” type, it involves a shoot and an epigonium. In both of the types, the sporophyte penetrates into an epigonial tissue accompanied by degeneration of epigonium cells under the developing sporophyte. In the “shoot vaginula” type, the sporophyte further penetrates into the conducting strand or similar cells that seem to be induced by stimulation of fertilization. It is likely that the difference in growth rate between the epigonium and the capped sporophyte is a mechanical force for sporophyte penetration.     

The development of the placenta in the anthocerote Phaeoceros laevis (L.) Prosk

The development of the placenta in the anthocerote Phaeoceros laevis (L.) Prosk. was studied by transmission electron microscopy. By the time the sporophyte emerges from the involucre, a conspicuous placental region is formed by the intrusive growth of sporophyte foot haustorial cells into the adjacent gametophyte vaginula tissue. The separation of gametophyte cells by haustorial cells and their incorporation into the placenta are preceded by the loosening and swelling of their walls and the formation of a periplasmic space. This process causes the disruption of the plasmodesmata, and may eventually result in the complete isolation and consequent degeneration of the cells. Crystals are commonly observed in the vacuoles of gametophyte placental cells. Crystals become more abundant during cytoplasmic degeneration, and are released in the placental lacunae that result from the complete dissolution of gametophyte cells. During the subsequent phase of capsule elongation, the gametophyte placental cells that retain the symplastic connection with the adjoining gametophyte parenchyma develop a wall labyrinth typical of transfer cells. Obliteration of the wall labyrinth by deposition of lightly staining wall material is observed later in sporophyte development, in concomitance with capsule dehiscence. Crystals are negative to the periodic acid/thiocarbohydrazide/silver proteinate test for carbohydrates whilst they are completely digested by pepsin or protease, denoting protein composition.Abbreviation PATAg periodic acid/thiocarbohydrazide/silver proteinate     

Transfer cells in the sporophyte — gametophyte junction ofPhyscomitrium cyathicarpum Mitt.

Summary Ultrastructural investigations reveal the presence of transfer cells in tissues belonging to both generations at the sporophyte-gametophyte junction. The foot epidermal cells possess an organelle-rich cytoplasm whereas cells of the vaginula contain more elaborate wall labyrinth. Also visible are differences in the extent of retraction of cytoplasm in these two types of cells.     

Physiological Aspects of Sugar Exchange between the Gametophyte and the Sporophyte of Polytrichum formosum

The sporophyte of bryophytes is dependent on the gametophyte for its carbon nutrition. This is especially true of the sporophytes of Polytrichum species, and it was generally thought that sucrose was the main form of sugar for long distance transport in the leptom. In Polytrichum formosum, sucrose was the main soluble sugar of the sporophyte and gametophyte tissues, and the highest concentration (about 230 mm) was found in the haustorium. In contrast, sugars collected from the vaginula apoplast were mainly hexoses, with traces of sucrose and trehalose. p-Chloromercuribenzene sulfonate, a nonpermeant inhibitor of the cell wall invertase, strongly reduced the hexose to sucrose ratio. The highest cell wall invertase activity (pH 4.5) was located in the vaginula, whereas the highest activity of a soluble invertase (pH 7.0) was found in both the vaginula and the haustorium. Glucose uptake was carrier-mediated but only weakly dependent on the external pH and the transmembrane electrical gradient, in contrast to amino acid uptake (S. Renault, C. Despeghel-Caussin, J.L. Bonnemain, S. Delrot [1989] Plant Physiol 90: 913-920). Furthermore, addition of 5 or 50 mm glucose to the incubation medium induced a marginal depolarization of the transmembrane potential difference of the transfer cells and had no effect on the pH of this medium. Glucose was converted to sucrose after its absorption into the haustorium. These results demonstrate the noncontinuity of sucrose at the gametophyte/sporophyte interface. They suggest that its conversion to glucose and fructose at this interface, and the subsequent reconversion to sucrose after hexose absorption by haustorium cells, mainly governs sugar accumulation in this latter organ.     

Morphology versus molecules in moss phylogeny: new insights (or controversies) from placental and vascular anatomy in Oedipodium griffithianum

New data on the placenta and water-conducting cells of Oedipodium griffithianum challenge current ideas on moss phylogeny. The placental region in O.?griffithianum consists of cells with highly convolute wall labyrinths on both the sporophytic and gametophytic side. This type of placenta distinguishes an assemblage of mosses including Tetraphis, Buxbaumia and all arthrodontous mosses but is not found in basal lineages including polytrichopsid mosses. Other features that distinguish Oedipodium from polytrichopsid mosses are the foot entirely ensheathed by the parenchymatous tissue of the gametophyte vaginula, the lack of a necrotic foot tip, the lack of intercellular spaces in the foot parenchyma and the presence of typical bryopsid hydroids with uniformly thin cell walls in the leafy shoot. These results do not support molecular phylogenies resolving Oedipodium as the sister group to polytrichopsid mosses or to all peristomate mosses, but are compatible with a sister relationship to a clade encompassing Tetraphis, Buxbaumia and arthrodontous mosses.     

Localization of some Hydrolases and Succinate Dehydrogenase in the Sporophyte--gametophyte Junction in Physcomitrium cyathicarpum Mitt.

Three groups of hydrolases, viz., acid and alkaline phophatasesand esterases and a respiratory enzyme, succinate dehydrogenase,have been localized in the zone constituting the sporophyte-gametophytejunction in the moss Physcomitrium cyathicarpum Mitt. (Funariaceae).Increased respiratory and phosphatase activities in the transfercells of the haustorial foot and vaginula implicate these cellsin active transport. Physcomitrium cyathicarpum Mitt., sporophyte-gametophyte junction, haustorial foot, hydrolases, succinate dehydrogenase, transfer cells, active transport     

Epidermal derivatives as xylem elements and transfer cells: a study of the host-parasite interface in two species of Triphysaria (Scrophulariaceae)

Summary Haustoria ofTriphysaria pusilla andT. versicolor subsp.faucibarbata from a natural habitat were analysed by light and electron microscopy. The keel-shaped edge of the secondary haustorium generally splits the epidermis and cortex of the host root parallel to the root axis, and penetrates to the host vascular tissue. Anticlinally elongated epidermal cells of the haustorium constitute most of the host/parasite interface. Some of these epidermal cells are divided by oblique cell walls. Some of their oblique daughter cells as well as some undivided epidermal cells differentiate into xylem elements. Single epidermal cells occasionally intrude into the vascular tissue of the host and individual host cells can be invaded. The surface area of the plasmalemma in parasitic parenchymatous interface cells is increased by the differentiation of wall labyrinths characteristic of transfer cells and by the development of membrane-lined cytoplasmic tubules or flattened sacs which become embedded in the partly lignified interface cell-wall. Mycorrhizal fungal hyphae enter the xylem bridge in some haustoria. Implications of these observations for the function of the haustorium are discussed.     

Single-stranded DNA transforms plant protoplasts

Summary The transfer of the Agrobacterium T-DNA to plant cells involves the induction of the Ti plasmid virulence genes. This induction results in the generation of linear single-stranded (ss) copies of the T-DNA inside Agrobacterium and such molecules might be directly transferred to the plant cell. A central requirement of this ss transfer model is that the plant cell must generate a second strand and integrate the resulting double-stranded (ds) molecule into its genome. Here we report that incubating plant protoplasts with ss or ds DNA under conditions favouring DNA uptake results in transformation. The frequencies of transformation are similar and analysis of ss transformants suggests that the introduced DNA becomes double stranded and integrated. Analysis of transient expression from introduced ss DNA suggests that generation of the second strand is rapid and extrachromosomal.     

Structure and Function of Transfer Cells in the Sporophyte Haustorium of Funaria hygrometrica Hedw: I. THE DEVELOPMENT AND ULTRASTRUCTURE OF THE AUSTORIUM

The development of the sporophyte-gametophyte interface in themoss, Funaria hygrometrica Hedw., is described with the aidof light- and electron-microscopy. The outer walls of the cellsthat abut the haustorial cavity in both generations developlabyrinths typical of transfer cells. This feature is more apparentin the epidermal cells of the sporophyte foot (haustorium),where development can be split into three main stages. The primarygrowth stage, which is complete at about the time the calyptradetaches from the ripened archegonium, involves the formationof transfer cells. The secondary stage is characterized by thedeposition of amorphous inclusions in the wall labyrinth ofthe transfer cells. The tertiary stage, which commences as thesporophyte capsule ripens, entails de-differentiation of thetransfer cell wall labyrinth to form a thick, heavily encrusted,outer cell wall. The pattern of development of these cells iscorrelated with changes in gametophyte- sporophyte translocationcapabilities.     

Morphology and development of rhabdovirus-like particles inCuscuta odorata (Convolvulaceae) simultaneous infected with virus and mycoplasma-like organisms

Summary Electron microscopic examination ofCuscuta odorata, used for transmission trials, revealed mycoplasma-like organisms (MLO) as well as rhabdovirus-like particles, unknown toCuscuta. The virus infection is confined to certain phloem-parenchyma cells and a 1–2 cell thick layer of parenchyma cells with thickened walls surrounding the central cylinder. Virus particles, mostly bacilliform, could be detected mainly in the nucleus but also in the cytoplasm. They reach a length of 350–400 nm and a diameter of approximately 75 nm. Virus assembly takes place exclusively in the nucleus. Virus maturation occurs in membrane bound areas within the nucleus, which have no connection with the perinuclear space. Formation of nucleocapsids is always associated with a nuclear viroplasm. Envelopment of virus particles occurs in these membrane bound areas. Budding into the perinuclear space does not occur. Virus infection leads to degeneration and finally to death of the protoplast.Abbreviations cy cytoplasm - m membrane stacks - mt mitochondria - my mycoplasma-like organisms - nc nucleocapsid - ncp nucleocapsid particles - nf nuclear filaments - np nucleoplasm - nu nucleus - nvp nuclear viroplasm - oc obliterated cells - p plastid - pc passage cells - ph phloem - ps perinuclear space - spc strand of parenchymatous cells - v virus particle - x xylem     

Embryology of Ceratopteris richardii (Pteridaceae, tribe Ceratopterideae), with emphasis on placental development

This comprehensive study of early embryology in Ceratopteris richardii combines light microscopy with the first ultrastructural evaluation of any pteridophyte embryo. Emphasis is placed on ontogeny of the foot and placental transfer cells. The embryology of C. richardii shares many similarities with that of other polypodiacious ferns while exhibiting distinctive division patterns. Formative embryonic stages have been reconstructed into three-dimensional models for ease of interpretation. The zygote divides perpendicular to the gametophyte plane and anterioposterior axis. This division establishes a prone embryological habit that maximizes rapid independent establishment of a leaf-root axis in a cordate gametophyte. After the formation of a globular eight-celled stage, initials of the first leaf, and root and shoot apical meristems are defined early by discrete formative divisions. Concomitantly, the foot expands and differentiates to transport nutrients from the gametophyte for the developing embryonic organs. Transfer cell wall ingrowth deposition begins in the gametophyte placental cells before the adjacent sporophyte cells just after the eight-celled stage. These observations provide an anatomical framework for future comparative developmental genetic studies of embryogenesis in free-sporing plants.     

INTERSPECIFIC INCOMPATIBILITY IN GOSSYPIUM. I. STEM HISTOGENESIS OF G. HIRSUTUM X G. GOSSYPIOIDES

The hybrid of Gossypium hirsutum X G. gossypioides develops normally until 10–12 nodes have been produced at which time neoplasms form in the cortex, phloem, and pith of the lower portion of the shoot axis. Neoplasms are characterized by irregular whorls of unusually large cells the central portions of which contain apparently cytolysed cells and a reddish-brown substance that probably represents the products of cytolysis. Neoplastic invasion is followed by inactivation of the vascular cambium, disorganization of the phloem and cortex, and tylosing and plugging of many xylem vessels. Subsequent growth of the shoot, which continues at a very slow rate for up to several years, involves the proliferation of parenchymatous tissue which becomes secondarily vascularized.     

Comparative anatomy of Sirhookera (Orchidaceae) growing in Western Ghats of southern India

We compared the anatomical characteristics of vegetative organs, peduncle and mycorrhizal morphology of the two known species of Sirhookera (Epidendroideae, Orchidaceae) to identify anatomical markers for identification and the ecological adaptations of these species. The leaves are hypostomatic bearing tetracytic stomata and the walls of subsidiary cells are smooth in Sirhookera lanceolata and undulate in Sirhookera latifolia. On the adaxial and abaxial surfaces the leaves are covered by a thick cuticle. The hypodermis is dimorphic and present on both sides of the leaf; chlorenchyma is homogenous and the vascular bundles are collateral. The rhizome of Sirhookera possesses a single-layered epidermis, thick cuticle, thin-walled parenchymatous ground tissue containing starch grains and scattered collateral vascular bundles. A thick-walled sclerenchymatous band separates the cortex from the parenchymatous ground tissue comprising of banded cells in the peduncle. Starch grains are present in the ground tissue of the S. latifolia peduncle. The roots consist of the velamen, ∩-thickened exodermis, thin-walled cortex consisting of water-storage cells, O-thickened endodermis and a vascular cylinder with parenchymatous pith. Starch grains are present in the root cortical cells of S. lanceolata but absent in S. latifolia. Fungal pelotons that aids in nutrient acquisition were observed in the root cortical region of both species. The study revealed significant differences between the anatomical characteristics of the two species and that most of the anatomical features of Sirhookera relate to their ecological adaptations.     

Ultrastructural and cytochemical aspects of induced apogamy following abscisic acid pre-treatment of secondary moss protonema

Abscisic acid (ABA) treatment of secondary protonema of Physcomitrium pyriforme Brid in the presence of sucrose does not prevent cell division but results in shorter cells with vesicular cytoplasm and an accumulation of lipid. When transferred to sucrose medium without ABA and with low irradiance isodiametric intercalary cells are cut off which give rise to apogamous sporophytes either directly or after the formation of a small amount of callus. The organization of the cells leading up to the apogamous sporophyte is described. The cells initiating the sporophyte develop dense cytoplasm and the walls become labyrinthine and callosed, but they do not form any recognizable placenta. It is proposed that labyrinthine walls are a consequence of a perturbation of cell wall metabolism as growth changes from gametophytic to sporophytic. The use of the term transfer cell for this kind of cell is questioned and the need for a causal approach to the investigation of labyrinthine walls is stressed.     

Ploidy chimeras induced in haploid sporophytes of <Emphasis Type="Italic">Osmunda claytoniana</Emphasis> and <Emphasis Type="Italic">Osmunda japonica</Emphasis>

Haploid sporophytes of Osmunda claytoniana (2n = x = 22) were apogamously produced from calli when cultivated on a hormone-free medium. Flow cytometric analysis showed that ploidy chimeras were spontaneously produced in a haploid sporophyte of O. claytoniana and those of O. japonica that were obtained in the previous study. In the haploid sporophyte of O. claytoniana, a diploid pinnule and a partially diploid terminal segment were produced in a haploid pinna. In O. japonica, a haploid sporophyte yielded a diploid pinna in a haploid frond, and another haploid sporophyte yielded a diploid pinnule in a haploid pinna. Diploid chimeras were large in size and could be readily distinguished from other haploid parts of the fronds. It is likely that the chimeras were produced clonally from a single diploid cell that established chromosome doubling.     

STEM ANATOMY OF PARTHENIUM ARGENTATUM,P. INCANUM AND THEIR NATURAL HYBRIDS

Guayule (Parthenium argentatum Gray) contains rubber in the parenchymatous cells of stems and roots. Stem anatomy of P. argentatum is described along with that of P. incanum H.B.K. (mariola). Anatomy of these species differs significantly. Phloem rays in both species increase in width by cell division and expansion; however, the increase observed in mariola is less as compared to that in guayule. Axial xylem parenchyma in guayule is generally a two-cell strand as compared to the fusiform axial xylem parenchyma observed in mariola. Vascular ray cells and cells of the pith region of guayule are parenchymatous, whereas those of mariola are sclerenchymatous. As a result of introgression between guayule and mariola, three forms of guayule exist in the native stands of Mexico. Morphological differences between these guayule plants have been described previously. The stem anatomy of these three groups of plants differ importantly. Group I guayule plants, least introgressed by mariola, have taller rays with the cells of pith region and vascular rays parenchymatous. Group III plants, highly introgressed by mariola, have a few to many cells of vascular rays and pith with lignified secondary walls and shorter rays. Many of the anatomical characteristics of group II plants, somewhat introgressed by mariola, are intermediate between group I and III plants.     

The Endophytic System of Arceuthobium minutissimum, the Indian Dwarf Mistletoe

The Indian dwarf mistletoe, Arceuthobium minutissimum Hook f.is the most diminutive dicotyledonous stem parasite on Pinusexcelsa. The endophytic system is well developed, having a largenumber of anastomosing strands in the cortex and sinkers penetratingthe medullary rays in wood. The cortical strand is protostelicwith the central tracheary elements, the vessels, surroundedby paren-chymatous cells. An earlier report of absence of vesselsseems to be erroneous. The growth of the cortical strands iseffected by an apical cell. The sinkers typically associatedwith the rays of host, are composed of parenchymatous cellsand tracheary elements including vessels. They make contactswith the cells of the ray through pits present in the trachearyelements. The sinkers cause hypertrophy and even fusion of twoor more rays to form a composite medullary ray. The tracheidsof the host tissue also become stunted and contorted in shape.These observations are in agreement with those of other investigatorson American host species for Arceuthobium.     

A probable pteridosperm from the uppermost Devonian near Ballyheigue, Go. Kerry, Ireland

A new genus of pleridosperms is described from the uppermost Devonian beds from Ballyheigue, Ireland. I.aceya hibernica May & Mat ten is represented by stems bearing spirally arranged fronds. The base of the frond is swollen and is about the same size as the stem. Pinnae are borne alternately and apparently in one plane on the rachis. The anatomy of the stem reveals a three-fluted protostele. Secondary xylem consists of rays and trachcids and secondary phloem is present. The inner cortex contains probable secretory and/or sclerotic cells. The outer cortex is of the spargaimm-type. Rachial trace formation is described. The U-shaped xylem strand of the rachis lacks secondary tissue. Pinnae traces are V- to C-shaped. A presumed adventitious root has a triarch protostele, a parenchymatous cortex and lacks a 'sparganum' outer zone. I.aceya is believed to be a member of the Lyginopleridaceae. The divisions of the sympodial protoxylem strand forming the rachial trace is compared among the Aneurophytales, Buteoxylonaceae, Calamopityaceae and Lyginopteridaceae and is shown to be similar.