Structural and Cytochemical Characteristics of the Stigma and Style in Vitis vinifera L. var. Sangiovese (Vitaceae)

Studies were carried out on structural and cytochemical aspectsof the stigma and style ofVitis vinifera . The stigma is ofthe wet papillate type with a continuous cuticle and pellicle.During the development of the papillae, the cell walls increasein thickness and produce a secretion product constituted oflipids that pass through the wall forming the exudate. The styleis solid with a central core of transmitting tissue which hasconspicuous intercellular spaces that increase remarkably fromthe periphery to the centre where the cuticle is present. Theintercellular spaces, where the pollen tubes grow, contain amatrix that includes polysaccharides, pectic substances andscattered areas of lipidic nature. Cytochemistry; stigma; style; ultrastructure; Vitis vinifera     

Heterostyly inPrimula. 1. Fine-structural and cytochemical features of the stigma and style inPrimula vulgaris huds

Summary The stigmas of the heterostylous genusPrimula are of the dry type without a free-flowing surface secretion. The papillae of the stigma surface cells of the two morphs, in pin (stigma exserted) and thrum (stamens exserted), bear a thin proteinaceous surface pellicle, overlying a discontinuous cuticle. The vacuoles of the papillate cells contain tannins, and tannin cells extend in files through the stigma heads and form a loose sheath surrounding the pollen-tube transmitting tract in the styles. The cells of the transmitting tissue in the stigma heads have a normal complement of organelles, and abundant ribosomal endoplasmic reticulum. The intercellular spaces contain an internal secretion which reacts cytochemically for both carbohydrate and protein. The transmitting tract in the styles forms a central core surrounded by several vascular strands. The cells are elongated, and the intercellular spaces here also have a carbohydrate-protein content. In a compatible pollination, thrum pollen tubes enter the stigma by penetrating the cuticle at the tip or on the flank of the pin papilla. Pin tubes on the thrum stigma enter between adjacent papillae, penetrating the thin cuticle at the base. The tubes grow through the transmitting tracts in the intercellular material.     

Structural studies of pollen tube growth in the pistil ofStrelitzia reginae

Summary For this work we have used various microscopical methods (LM, SEM, and TEM) to study pollen tube growth and interaction with the transmitting tisse inStrelitzia reginae, which has an open style. By the use of SEM it was possible to trace the exact route of the pollen tubes in the ovary of this plant and demonstrate that they exclusively follow the outlines of the transmitting tissue. The average rate of pollen tube growth through the style was 1.8 mm h^–1. The most significant effect of the pollination was a thickening of the distal wall of the subepithelial cells in the style. A secretion covers the stigma and the ovarian transmitting tissue and fills the stylar canal. This exudate contains lipids, polysaccharides, and proteins.     

Pollen-pistil Interaction in a Non-pseudogamous Apomict,Commiphora wightii

Structural and cytochemical details of the pistil and the interactionof pollen and pistil were studied in a non-pseudogamous apomict,Commiphorawightii.The anthers in the male and bisexual flowers producefunctional pollen grains. The stigma is of the wet and papillatetype. The style is typically solid with two strands of transmittingtissue that traverse the entire length of the style. There isa marked reduction in the area occupied by the transmittingtissue from the stigma to the base of the style. The cells ofthe transmitting tissue are isodiametric in transverse as wellas longitudinal section and do not form longitudinal files ofelongated cells as reported for other taxa. Proteins could notbe localized in the intercellular matrix. Although pollen grainsgerminate on the stigma, pollen tubes do not grow beyond theproximal one third of the style. Changed orientation of thecells of the transmitting tissue and absence of proteins inthe intercellular matrix could account for the failure of thepistil to support pollen growth.Copyright 1998 Annals of BotanyCompany Guggul, pollen-pistil interaction, non-pseudogamous apomict,Commiphora wightii, transmitting tissue     

Divergent pollination systems in the cleistogamous species,Collomia grandiflora (Polemoniaceae)

Summary A structural study of pollination in the dimorphic flowers ofCollomia grandiflora, a cleistogamous species, reveals significant differences in stigma behavior during pollination, stylar structure, the timing of generative cell division, and pollen tube growth rate patterns. The cleistogamous flower shows a loss of protandry and the stigma is receptive only after reflexing and closing of its lobes. In contrast, the chasmogamous stigma is receptive when reflexed and closes when pollen has been deposited on the lobes. Pollen tube penetration of the dry stigma papillae and entry into the style is similar in the two morphs. The chasmogamous style is solid and the cleistogamous style partly hollow. The matrix of secretion produced by the transmitting tract cells is mainly carbohydrate with a trace of lipids. It is fibrillar in nature and appears to be partly comprised of wall material from the transmitting tract cells. In the chasmogamous pollen, the generative cell enters the tube before division, which occurs between 30 and 60 min after pollination. This division correlates with an increased growth rate for the pollen tube. In the cleistogamous pollen, contact with the stigma triggers generative cell division inside the hydrated pollen grain before germination. The two resulting sperm cells exit the grain 15–30 min after pollination when the pollen tube is in the stigma lobes. The cleistogamous pollen tube shows only one phase of growth which occurs at a rate similar to that of the slow, first phase of the chasmogamous pollen.Abbreviations CH chasmogamous - CL cleistogamous - DAPI 4, 6-diamidino-2-phenylindole     

The Transmitting Tissue in Brugmansia suaveolens L.: Ultrastructure of the Stylar Transmitting Tissue

The stylar transmitting tissue of the angel's trumpet, Brugmansia(Datura) suaveolens, was studied at two developmental stages:about 6 d before anthesis and after anthesis. Histochemicallocalization of polysaccharides was carried out with PATAg andimmunohistochemistry with gold-conjugated antibodies recognizingpectins. Before anthesis the transmitting tissue forms a centralcore of polyhedral meristematic, still dividing, cells withnarrow intercellular spaces. Epitopes for unesterified pectinsare present in the walls and the spaces between the cells, whilemethylesterified pectins are confined to the middle lamellaand intercellular spaces. PATAg positive material and the antibodyagainst unesterified pectin was found in plasmalemma invaginationsand multivesicular bodies. Dictyosome cisternae and vesiclescontained epitopes for both kinds of pectins. Plastids are poorlydifferentiated and lack starch. Nutrients are stored as lipidbodies, which are digested by small vacuoles. After anthesisthe transmitting tract cells form cylindrical files separatedby voluminous spaces filled with a mucous secretion reactingwith PATAg and with the antibody against unesterified pectins.Dictyosome vesicles contain epitopes for the same kind of pectins.The cells are vacuolized and have leucoplasts. This study showspectin synthesis by different parts of the endomembrane systemand changes in pectin esterification during stylar development.Copyright1993, 1999 Academic Press Brugmansia suaveolens, immunocytochemistry, pectin, secretion, style, transmitting tissue     

Developmental Aspects of Ultrastructure and Histochemistry of the Stylar Transmitting Tissue of Nicotiana sylvestris

The structure and histochemistry of the solid style of Nicotiana sylvestris Speg. and Comes have been studied by light and electron microscopy. The transmitting tissue develops large intercellular spaces filled with secretions rich in proteins and carbohydrates during maturation. The cells possess large nuclei, numerous plastids with starch grains, mitochondria, ribosomes and well developed endoplasmic reticulum and golgi apparatus. The plastids in the stylar region immediately below the stigma produce electron-dense osmiophilic substances which are probably transferred into the cytoplasm by a process resembling budding-off of vesicles. The Golgi apparatus may use the starch grains as a source of sugars for the synthesis and secretion of extracellular polysaccharides. The structural and cytochemical differences between the glandular cells of the stigma and the stylar transmitting tissue are discussed.     

The Structure and Cytochemistry of the Pistil of Hypericum calycinum: The Stigma

The pistil of Hypericum calycinum has a pentacarpellary, syncarpousovary with five slender styles, each terminating in a smallstigma. The stigma is dry and papillate with a thin lining ofpellicle. The cuticle is thin and continuous around the papillae.A large vacuole filled with tannins occupies the major partof the papillae and the cytoplasm forms a thin lining aroundthe vacuole. The cell wall of the mature papillae show two distinctlayers - an outer layer of loosely woven fibrils and an innerdenser layer with compact fibrils. A large number of small lipoidalbodies accumulate just below the cuticle. The papillae havefewer organelles than those typical of glandular cells. Dictyosomesobserved occasionally are without associated vesicles. The cytoplasmis rich in ribosomes. The basal portions of the papillae mergeinto the transmitting tissue made up of loosely arranged cells.The intercellular matrix of the transmitting tissue is richin lipids. Pollen grains are deposited between the papillae.Upon pollen germination, pollen tubes enter the stigma throughthe interstices between the papillae Hypericum calycinum, cytochemistry, pistil, pollen-pistil interaction, stigma, ultrastructure     

GYNOECIAL DEVELOPMENT,POLLINATION, AND THE PATH OF POLLEN TUBE GROWTH IN THE TEPARY BEAN,PHASEOLUS ACUTIFOLIUS

The gynoecium of Phaseolus acutifolius var. latifolius, a self-compatible legume, is characterized by a wet non-papillate stigma, an intermeditae hollow/solid style type, and secretory cells on the ventral surface of the ovary which direct pollen tube growth. The stigma is initially receptive 5–6 days prior to anthesis. Production of stigmatic secretions, composed primarily of carbohydrates and lipids, fragment the cuticle covering epidermal cells of the stigma early in ontogeny; the lipidic aspect of the copious secretions apparently serves to inhibit desiccation after the cuticle is ruptured. Stylar canal development occurs as a combination of elongation of a basal canal present early in development, and dissolution of part of a solid transmitting tract tissue just below the stigma. Anthers dehisce and the tricolporate pollen is released onto the receptive stigma one day before anthesis. Following initial growth in intercellular spaces in the transmitting tract of the stigma, pollen tubes adhere to epidermal secretory cells along the ventral side of the stylar canal and upper ovary; here the transmitting tract is apparently limited in the number of tubes it can accommodate, providing a possible site of selection of male gametes.     

Structure and Cytochemistry of the Stigma and Pollen--Pistil Interaction in Zephyranthes

The stigma in Zephyranthes candida and Z. citrina is of thedry type with a continuous cuticle—pellicle. In some papillae,however, the terminal portion of the cuticle—pellicleis lifted upwards and occasionally even disrupted by the accumulationof a secretion product below it. Both non-specific esterasesand acid phosphatases are present on the stigma surface. Thestyle is solid with a central core of transmitting tissue whichhas conspicuous intercellular spaces containing a matrix thatincludes proteins, polysaccharides and pectic substances. Zephyranthes citrina is self-compatible while Z. candida isself-incompatible. Followng incompatible pollination in Z. candida,pollen germination is normal but pollen tube growth is inhibitedat the junction of the stigma and style. Self-incompatibilitycan be overcome by bud pollination. Protein synthesis is necessaryfor pollen germination in both species. Concanavalin A bindsto the stigma surface of both species, but does not affect pollentube penetration in Z. candida. In crosses between the two speciestypical unilateral incompatibility is observed when Z. candidais used as the pistillate parent. Zephyranthes, stigma-surface enzymes, dry stigma, pollen-pistil interaction, self-incompatibility, unilateral-incompatibility     

Heterostyly inPrimula. 2. Sites of pollen inhibition,and effects of pistil constituents on compatible and incompatible pollen-tube growth

Summary In incompatible (intramorph) pollinations of the heterostylousPrimula vulgaris, pollen germination or tube growth may be partially inhibited in several sites associated with the stigma or style. Blockage may occur, a) on the stigma surface through the failure of germination or of pollen tube penetration after germination, b) in the stigma head during the passage of the tube through the specialized transmitting tissue of the head, or c) in the transmitting tract of the style. None of the barriers is complete, and the prohibition of selfing or intramorph crossing depends upon the cumulative screening effect of one following upon the other. In both morphs, the germination of incompatible pollen on the stigma is enhanced in high ambient relative humidity, but many tubes still fail to penetrate the stigma. Those that do are retarded or blocked in their growth in the transmitting tissues of the stigma head and style. Crude extracts from the tissues of the stigma head and style show some differential effect on the growth of pollen tubesin vitro, and dialysates of extracts containing high molecular weight fractions show a consistent differential effect, those from thrum tissues retarding thrum tubes while having a lesser effect on pin tubes, and those from pin tissues retarding pin tubes while having lesser effect on thrum. It is suggested that the factors influencing tube growth are present in the intercellular secretions of the transmitting tract.     

Pollen--stigma Interaction in the Leguminosae: the Secretory System of the Style in Trifolium pratense L.

The canal that traverses the upper part of the style of Trifoliumpratense is derived lysigenously. The core tissue of the veryyoung style consists of elongated cells similar to those ofthe transmitting tissue of solid-style families such as theSolanaceae; as the style matures, these cells separate to formthe canal, which receives secretions both from the core tissueand the inner wall cells. The early secretion of proteins intothe intercellular spaces is associated with the presence ofparamural bodies (lomasomes) in the adjacent cells. In the cellsin the immediate vicinity of the canal, vesicles, probably derivedfrom the Golgi system enlarge during later development and accumulatea protein-carbohydrate content, which is later passed into thecytoplasm where it forms densely packed fibrillar nodules. Withthe dissolution of the cell membranes, this material is passedinto the canal, where it is progressively diluted by continuedingress of water until the cavity reaches its final volume. Leguminosae, Trifolium pratense L., pollen—stigma interaction, self-incompatibility, stylar secretion, protein secretion     

Cotton embryogenesis: The tissues of the stigma and style and their relation to the pollen tube

Summary The stigma of cotton (Gossypium hirsutum) is covered by unicellular hairs. The cytoplasm of these hairs degenerates before the stigma becomes receptive. The vacuole remains intact, but the hair cytoplasm becomes a mass of dark, amorphous material with only a few organelles still being visible. The rest of the stigma consists of thin-walled parenchyma cells with large vacuoles and large amounts of starch. The cells of the style are differentiated into a uniseriate epidermis, vascular tissue, a cortex of thin-walled, vacuolate parenchyma cells, and the transmitting tissue. This latter tissue occupies the center of the style and consists of thick-walled cells with few vacuoles. The cells are rich in starch, ribosomes, endoplasmic reticulum and dictyosomes. They also contain deposits of calcium salts in the form of druses. The pollen germinates on the stigmatic hairs, grows down the outside of the hair and between the cells of the stigma to the transmitting tissue of the style. There the tubes grow between the walls of the cells but do not enter the cells themselves. Some transmitting cells adjacent to the pollen tube degenerate after the tip of the pollen tube has grown past them. However, not all degenerate, and those that do show no fixed spatial relationship to one another. The cells which do degenerate follow a characteristic pattern of breakdown. No ultrastructural evidence was found for the secretion of hydrolytic enzymes by the pollen tube.     

DYNAMICS OF POLLEN TUBE GROWTH IN THE WILD RADISH RAPHANUS RAPHANISTRUM (BRASSICACEAE). II. MORPHOLOGY,CYTOCHEMISTRY AND ULTRASTRUCTURE OF TRANSMITTING TISSUES,AND PATH OF POLLEN TUBE GROWTH

The relative importance of prezygotic mechanisms of gametophytic competition and selection are often unclear due to an absence of observations on the gynoecium and pollen tube growth in vivo. We used LM, SEM, and TEM to study the structure of the gynoecium and the path of pollen tube growth in Raphanus raphanistrum, a sporophytically self-incompatible annual. Wild radish has a papillate stigma and a solid style. A septum, which is characteristic of cruciferous gynoecia, is present in the ovary. After germination on the stigma, pollen tubes grow in the secretion of the transmitting tract of the style. The stylar secretion stains positive for acidic polysaccharides and insoluble carbohydrates, and negative for lipids and protein. In the ovary, the transmitting tissue is contained inside the septum. The secretion in the ovary stains positive only for acidic polysaccharides. Pollen tubes travel inside the septum as they enter the ovary and must exit to the surface of this tissue before ovule fertilization can occur. Pollen tube growth on the septum tracks the intercellular junctions of the septum epidermis where the secretion leaks out through a torn cuticle. Tubes must grow across the obturator before reaching the micropyle of an ovule. The temporal pattern with which tubes growing into the ovary exit the septum can contribute to the previously observed nonrandom patterns of fertilization (Hill and Lord, 1986).     

Transmitting Tissae and Pollen Tube Growth in Sweet Pepper

Fine structural events in the mature stylar transmitting tissue ofsweet pepper (Capsicum frutescens L. var. grossum Bally) have been investigated byelectron microscope with regard to pollen tribe grwoth. The transmitting tissue consists of parenchymatous cells with large intercellular spaces filled with an electron densesubstance. The pollen tubes grow through the intercellular spaces in the intercellular substance. Cells of this tissue are rich in organelles, especially the rough and tubular ER, and numerous lomasomes near the plasma membrane. It is demonstrated that they function as secretory cells. On the other hand, the fact that the transmitting tissue contains many large amyloplastids with several starch grains in the cytoplasm and numerous globular protein bodies in vacuoles, indicates that the transmitting tissue mayhave some nutritive value for the growth of pollen tubes. The results obtained from this observation are in agreement with those of mostspecies reported by other authors and support the conclusion that the transmitting tissue is not a collenchyma tissue and the nature of intercellular substances is essentially same as that of the middle lamella.     

Tissue organisation,pollen receptivity and pollen tube guidance in normal and mutant stigmas of the grass Pennisetum typhoides (Burm.) Stapf et Hubb.

Summary The normal stigma of Pennisetum typhoides is twin-branched, each branch bearing unbranched trichomes. As is general among the grasses, the papillate cells of the trichomes possess a discontinuous cuticle with overlying protein and polysaccharide secretions. These adaptations for pollen capture and hydration are absent from the stigma axes. Pollen tubes emerging from grains received on the trichomes are guided into the axes with the tips directed towards the ovary by the architecture of the basal cell complex. There are no defined transmitting tracts in the stigma axes, and further passage is through intercellular spaces of a tissue of elongated cells between the epidermis and the central vascular strands. In the mutant tr, tr, the stigmas are twin-branched, but lack trichomes. However, the principal adaptations of the trichome cells for the capture and hydration of pollen are expressed in the epidermal cells of the branches, which have permeable cuticles and the characteristic surface secretions. Pollen tubes emerging from grains germinating on the branches enter between the files of epidermal cells, or at their ends. In the absence of the guidance provided by trichome structure in the normal stigma, they pass indifferently either towards or away from the ovary. The implications of the comparison between the normal and mutant genotypes for understanding the requirements for pollen capture, germination and pollen-tube guidance in the grasses are discussed.     

Changes of pH in <Emphasis Type="Italic">Petunia hybrida</Emphasis> (Hort.) styles induced by pollination and influence of proton pump and ion channels on its regulation

Ionselective microelectrode method was used to study changes of pH in transmitting tissue of style in Petunia hybrida (Hort.). Effect of pollination and pollen tube growth were examined. Subsequently solutions of ions and various stimulators or blockers of ion channels were applied on pollinated styles to examine the possible role of ion channels in pH stabilisation. It was confirmed in the present study that: (1) there is a pH gradient in the transmitting tissue of a petunia unpollinated style with the stigma region being more acidic; (2) pollination causes further acidification of transmitting tissue: (3) the gradient of pH first vanishes at 24 h after pollination then is reversed up to 72 h after pollination; (4) active transport of ions plays an important role in pH regulation in transmitting tissue. The presented results confirm the role of pH changes and Ca²⁺ as a mediator in controlling proton influx into the apoplast of the transmitting tissue during pollen tube growth.     

Stigmatic and stylar incompatibility in Prunus avium L.: Morphological and ultrastructural aspects

Abstract

Stigmatic and stylar structures of-sweet cherry (Prunus avium L.) «Malizia» were examined with light and electron microscopes (S.E.M. and T.E.M.).

It was demonstrated that the transmitting tissue, situated in the central portion of the style, extends below the stigmatic papillae and secretes an electrondense material accumulating in the intercellular spaces. Pollen tubes which germinated on the stigma, reached the ovules passing through this substance which facilitates their passage while trophic relations are established.

Some ultrastructural aspects of the pollen tubes observed inside the style were examined and discussed in relation to the phenomenon of self-incompatibility.     

Pollen-pistil interaction in kiwifruit (Actinidia deliciosa; Actinidiaceae)

The pollen-pistil interaction has been examined in kiwifruit (Actinidia deliciosa). In this species a large number of seeds are produced in each fruit and a great many pollen grains germinate and grow to reach the ovules. This growth is assisted by an abundant secretion that is present all along the pistilar tract. At anthesis, the stigma is covered by a secretion where the pollen grains germinate and grow. The stylar transmitting tissue is initially rich in starch reserves, but the starch gradually disappears and, concomitantly, an abundant secretion that stains for carbohydrates appears in all of the intercellular spaces. Pollen tube growth relies on this secretion since it is depleted after pollen tube passage, while in unpollinated flowers it remains unaltered throughout the flower life-span. In the ovary a similar situation occurs. The placental surface, where the pollen tubes grow before reaching the ovules, is covered by a number of obturators. At anthesis, these obturators are rich in starch reserves and have an abundant secretion on their outer surface. As time passes, starch disappears while the secretion increases. It is in this secretion that the pollen tubes grow on their way toward the ovules. These observations are discussed in terms of the support given by the pistil to pollen tube growth to achieve the highly successful reproductive performance of this species.     

Pollen tube growth and the pollen‐tube pathway of Nymphaea odorata (Nymphaeaceae)

An important aspect of the evolution of carpel closure, or angiospermy, is the relationship between pollen tube growth patterns and internalization of the pollen‐tube pathway. True carpel closure, involving postgenital fusion of inner carpel margins, is inferred to have arisen once within the ancient order Nymphaeales, in the common ancestor of Nymphaeaceae. We studied pollen tube development, from pollination to fertilization, in a natural population of Nymphaea odorata, using hand pollinations and timed flower collections. Pollen germinates in stigmatic secretions within 15 min and pollen tubes enter subdermal transmitting tissue within an hour, following wide intercellular spaces towards the zone of postgenital fusion. At the zone of fusion they turn downwards to grow in narrow spaces between interlocked cells and then wander freely to ovules within ovarian secretions. The pollen‐tube pathway is 2–6 mm long and upper ovules are first penetrated 2.5 h after pollination. Pollen tubes grow at rates of approximately 1 mm/h whether in stigmatic fluid, transmitting tissues or ovarian secretions. Pollen‐tube pathways are structurally diverse across Nymphaeales, yet their pollen tubes have similar morphologies and rapid growth rates. This pattern suggests pollen tube growth innovations preceded and were essential for the evolution of complete carpel closure. © 2010 The Linnean Society of London, Botanical Journal of the Linnean Society, 2010, 162 , 581–593.