White Vesicles in the Skin of Aplysia californicaCooper: A Proposed Excretory Function

White patches of skin that appear early in the development ofthe shell-less mollusc, Aplysia californica, are composed ofaggregations of vase-shaped vesicles, each a single, large cellwith an enlarged nucleus. Two layers of collagen, at 90°to each other, surround the vesicle membrane, together witha non-contiguous external layer of muscle. Energy dispersivespectroscopy and electron diffraction of the contents with scanningelectron microscopy (SEM) and transmission electron microscopy(TEM) failed to find a signal for halogens (involved with unpalatableskin and, therefore, defence against predation), but did recordprominent signals for calcium. Immature vesicles are filledwith an homogenous material that appeared to mature progressively,likely by nucleation, into numerous, small spherules, visibleby both SEM and TEM. Ultra-thin uranyl acetate stained sectionsof mature vesicles showed that the spherules had an intracrystallinematrix of radially arranged electron-dense material. The vesiclecell had none of the modifications characteristic of calciumor rhogocyte cell-types, which serve as calcium reservoirs forthe movement of this element to sites of shell formation andregeneration. These vesicles are likely involved with the excretionof excess calcium and not, as originally hypothesized, witheither defence against predators or calcium flux. In addition,the spherules that fill the vesicles are possibly composed ofthe less common polymorphs of calcium carbonate, vaterite andamorphous calcium carbonate. Excretion of the vesicle contentsappeared to be passive, since vesicles lacked an abundant contiguouslayer of muscle or a muscular release valve in the vesicle neck,but did have organized layers of collagen just outside the vesiclemembrane. We propose that release of vesicle contents probablyoccurs when the neck of the vesicle is broken. (Received 5 December 2005; accepted 28 April 2006)     

Histological description of the ink gland of the tropical sea hare Aplysia dactylomela Rang, 1828

This work describes for the first time the ink gland of Aplysia dactylomela Rang, 1828 using light microscopy and histochemical tests. The results reveal that this organ is covered by a layer of simple epithelium and that there are some differences between the epithelium facing the mantle shelf and that facing the mantle cavity. The former consists of columnar cells, which may have a secretory function, whereas the latter is a cuboidal epithelium. Underneath the epithelium and along the whole gland there are fibres of smooth muscle and collagen, organized in groups of parallel bundles. There are vesicles of different diameters, apparently with similar morphology. Some are filled with ink, whereas others are either granular or clear. The ink is released through a duct formed by invaginations of the cuboidal epithelium. Tests with bromophenol blue and periodic acid Schiff indicated that the ink and granulated vesicles contain proteins and carbohydrates or maybe glycoproteins. Between the fibre bundles and the vesicles there are dispersed cells. A diagram is presented emphasizing the covering epithelium, the distribution of muscle and collagen fibres, the dispersed cells, vesicles and ducts. This organization is similar to that of the other Aplysia species studied to date, A. californica.     

Acidity enhances the effectiveness of active chemical defensive secretions of sea hares, <Emphasis Type="Italic">Aplysia californica</Emphasis>, against spiny lobsters, <Emphasis Type="Italic">Panulirus interruptus</Emphasis>

Sea hares such as Aplysia californica, gastropod molluscs lacking a protective shell, can release a purple cloud of chemicals when vigorously attacked by predators. This active chemical defense is composed of two glandular secretions, ink and opaline, both of which contain an array of compounds. This secretion defends sea hares against predators such as California spiny lobsters Panulirus interruptus via multiple mechanisms, one of which is phagomimicry, in which secretions containing feeding chemicals attract and distract predators toward the secretion and away from the sea hare. We show here that ink and opaline are highly acidic, both having a pH of ∼5. We examined if the acidity of ink and opaline affects their phagomimetic properties. We tested behavioral and electrophysiological responses of chemoreceptor neurons in the olfactory and gustatory organs of P. interruptus, to ink and opaline of A. californica within their natural range of pH values, from ∼5 to 8. Both behavioral and electrophysiological responses to ink and opaline were enhanced at low pH, and low pH alone accounted for most of this effect. Our data suggest that acidity enhances the phagomimetic chemical defense of sea hares.     

Ultrastructural comparison of Aplysia and Dolabrifera ink glands suggests cellular sites of anti-predator protein production and algal pigment processing

Ultrastructural comparison between the ink gland of a sea harespecies that produces copious purple ink (Aplysia californica)and one that produces none (Dolabrifera dolabrifera), suggeststhat the rough endoplasmic reticulum rich cell and not the inkvesicle cell is the site for synthesis of A. californica's anti-predatorink protein, escapin. Dolabrifera dolabrifera were found tohave vestigial ink glands incapable of producing ink or itsassociated anti-predator proteins regardless of diet. This studyalso suggests that the granulate cells serve only as a storagesite for excess ink pigment acquired during periods of luxuryfeeding on red algae. Slit dimensions in sieve areas of granulatecells are also significantly different between the two species.These slit sizes are larger than those of rhogocytes, a relatedcell type commonly found in connective tissue of gastropod molluscs.Several traits of granulate cells suggest that they are distinctfrom rhogocytes and are a special cell type in the ink glandof sea hares. (Received 1 July 2005; accepted 1 April 2006)     

Multiple components in ink of the sea hare Aplysia californica are aversive to the sea anemone Anthopleura sola

Sea hares of the genus Aplysia rely on an array of behavioral and chemical defenses, including the release of ink and opaline, to protect themselves from predation. While many studies have demonstrated that ink and opaline are repellent to predators, very little is known about which components of these secretions are active against predators. Ink was previously shown to facilitate the escape of Aplysia from predatory anemones (Anthopleura) by eliciting tentacle retraction and/or shriveling, and gastrovascular eversion, but the metabolites mediating this interaction were not identified. We investigated the metabolites in Aplysia californica secretions that were aversive to the anemone Anthopleura sola, as demonstrated by tentacle shriveling and/or retraction. We found that ink elicited tentacle shriveling and/or retraction, while opaline elicited a feeding response. The active components in ink do not appear to be diet-dependent, as ink was aversive regardless of diet (natural seaweed diet vs. Gracilaria ferox). Furthermore, metabolites extracted from G. ferox were not aversive, suggesting that the aversive components are produced by the sea hares. We then examined escapin, a protein in ink with antimicrobial properties. Escapin quickly forms reaction products when mixed with the amino acids l-lysine and l-arginine, which would occur when ink and opaline are released into the sea hare mantle cavity. Neither escapin alone nor escapin mixed with its amino acid substrate l-lysine elicited aversive behaviors either immediately before or 2 min before applying to the tentacles. In addition, escapin mixed with opaline and applied to tentacles after 2 min did not elicit a significant aversive response. Using bioassay-guided fractionation, we attempted to isolate the components in A. californica ink that are aversive to A. sola. We determined that multiple components in ink, including both lipophilic and hydrophilic constituents, elicited aversive responses. We hypothesize that these components may facilitate A. californica's escape from A. sola by eliciting tentacle shriveling and/or retraction, which lead to anemones dropping ensnared sea hares.     

Responses of the sea catfish Ariopsis felis to chemical defenses from the sea hare Aplysia californica

Ink secretion of sea hares (Aplysia spp.), which is a mixture of co-released ink from the ink gland and opaline from the opaline gland, protects sea hares from predatory invertebrates through diverse mechanisms. These include both aversive or deterrent compounds and also high concentrations of amino acids that stimulate the predators' chemical senses and divert the attack through phagomimicry or sensory disruption. The aim of the present study was to examine if sea hares also defend themselves from predatory vertebrates by interacting with their chemical senses. We used sea catfish, Ariopsis felis, in behavioral and electrophysiological experiments. Behavioral tests on sea catfish show that ink is aversive: when ink is added to palatable food items (noodles with food flavoring), the noodles are no longer eaten, and when ink is added to noodles without food flavoring, the noodles are avoided more than unflavored noodles. Behavioral tests also show that opaline and the amino acid components of either opaline or ink are appetitive. Electrophysiological recordings of chemosensory neuronal activity in the olfactory epithelium and maxillary barbels show that the olfactory and gustatory systems of sea catfish are highly stimulated by ink and opaline, and that the amino acid components of ink and opaline significantly contribute to these responses. Compounds generated by the activity of escapin, an L-amino acid oxidase in the secretion, are moderately stimulatory to both olfactory and gustatory systems. Taken together, our results support the idea that sea hares are chemically defended from predatory sea catfish largely through unpalatable chemical deterrents in ink, but possibly also through amino acids stimulating olfactory and gustatory systems and thus functioning through phagomimicry or sensory disruption.     

Interspecific variation in chemical defenses in the sea hares (Opisthobranchia: Anaspidea)

Most species of sea hares (Opisthobranchia: Anaspidea) sequester secondary metabolites from their algal diets in their digestive glands. Aplysia Juliana Quoy and Gaimard, 1832, a sea hare that feeds on Ulva spp. and Enteromorpha spp., algae with few or no secondary metabolites, were compared with the sympatric sea hares A. oculifera Adams and Reeve, 1850, A. kurodai (Baba, 1937), and Dolabella auricularia (Solander, 1786), all of which eat chemically rich algae, to see if sequestered secondary metabolites afford protection to sea hares from potential predators. Organic extracts of whole A. Juliana stimulated, and organic extracts of whole D. auricularia deterred feeding by crabs. However, tests with organic extracts of individual body parts indicated that this pattern was due almost exclusively to unpalatability of extracts of D. auricularia digestive glands. Tests with pieces of tissue from the exterior of the animals, or with extracts of such tissues, showed no consistent patterns indicating that A. Juliana were more palatable than other sea hares. Sea hare egg masses do not appear to contain diet-derived secondary metabolites. However, pieces of egg masses of A. Juliana and D. auricularia were universally rejected by crabs and reef fish, and extracts of A. Juliana egg masses deterred feeding by some reef fish. Finally, both opaline secretion of A. Juliana and ink of A. kurodai, but not ink of D. auricularia, none of which appear to contain diet-derived secondary metabolites, deterred feeding by crabs. Opaline secretion from A. Juliana, but not ink from A. kurodai, induced avoidance behavior in crabs. Although sequestered secondary metabolites clearly can affect the palatability of the digestive gland, there is little evidence that they affect the palatibility of the ink, opaline secretion, eggs, or skin, suggesting that sequestered secondary metabolites may not play a key role in anti-predator defense of sea hares.     

曼氏无针乌贼墨囊组织学及墨汁形成的超微结构

采用组织学和电镜技术对曼氏无针乌贼的墨囊及墨腺细胞进行了研究。结果表明:墨囊壁和导管壁由外膜、肌肉层和黏膜三部分组成;墨腺体集中在墨囊底部,呈索状,腺体中部含丰富的结缔组织;墨汁颗粒以游离态形式分布于索状腺体的间隙及墨囊腔中。实验观察到无分泌黑色素功能的A型细胞和有分泌黑色素功能的B型细胞;在B型细胞中可见黑色素颗粒储存在囊泡中,囊泡在移出细胞的过程中逐渐变大,泡内的黑色素颗粒逐渐变多。囊泡可能通过胞吐的方式排出细胞外,黑色素排出后以颗粒的形式游离于细胞间隙中,形成墨汁。     

Ultrastructure of the copulatory organ of Haplopharynx quadristimulus and its phylogenetic significance (Plathelminthes,Haplopharyngida)

Summary The male reproductive system in Haplopharynx quadristimulus consists of paired testes, sperm ducts, seminal vesicles, seminal ducts, a copulatory organ containing prostatic vesicle and stylet apparatus, and the male canal. By electron microscopy all components appeared to be regional specializations of a canal extending from the testes to the body wall and lined by a multiciliated epithelium. The epithelium of the stylet apparatus contained six different cell types. One cell type (matrix syncytium) formed the stylet and the other five were located distal to the stylet/prostatic-vesicle junction along the male system epithelium. Each cell type was attached to the supporting intercellular matrix at a different level along the stylet apparatus. All cell types extended to the distal end of the stylet apparatus regardless of where they originated along its length. The cells in the apparatus lacked cilia, but one of the cell types contained rootlets. Modified rootlets or rootlet derivatives were possibly present in another cell type in the form of rootlet-like ribbons. The findings support the monophyly of the Macrostomida Haplopharyngida (by common occurrence of a matrix syncytium) and at the same time suggest their separation as two distinct taxa (by differences in the structure of the prostatic vesicle and other parts of the stylet apparatus).Abbreviations a accessory spine - c circular muscle - ce centriole - ci cilium - di dictyosome - e epithelial cell - ed ejaculatory duct - ep epidermal cell - f rootlet-like ribbon - g prostatic gland cell neck - g1 type I gland cell granules - g2 type II gland cell granules - g3 type III gland cell granules - h hemidesmosome - i intercellular matrix - im internal muscle - j septate junction - l stylet apparatus lumen - le spine lateral extension - lm longitudinal muscle - m matrix syncytium - mc male-canal epithelial cell - me male canal - mp male pore - mt microtubules - mv microvilli - n nucleus - nc nerve cell body - np nerve process - om oblique muscle - p prostatic vesicle epithelial cell - pv prostatic vesicle - r rootlet - s stylet - sa stylet apparatus - sc sensory receptor - sd sperm duct - se seminal duct - sl stylet lumen - sp spot desmosome - sr sperm - sv seminal vesicle - t terminal web - te testis - u ultrarhabdite - z zonula adhaerens - 2 cell type 2 - 3 cell type 3 - 4 cell type 4 - 6 cell type 6     

Biogenic Opal in Three Species of Gramineae

Particulate biogenic opaline silica is concentrated in cellwalls, intercellular deposits and cell lumina of all portionsof the above-ground plant body of three species of PanicoidGramineae,Andropogon gerardi, Sorgastrum nutans and Panicumvirgatum. Morphologically distinct opal phytoliths form notonly in long cells, short cells, trichomes, stomatal elementsand bulliform cells of the epidermis but also within the cellularstructure of mesophyll, vascular, and sclerenchyma tissues.Roots and rhizomes contain measurable quantities of opalinesilica, and phytoliths develop in epidermal long cells, saddle-shapedshort cells, vascular cells, and intercellular deposits. A morphologicallyunique plate-phytolith, formed by silicification of the innertangential wall of the endodermis, is present in the roots ofall three species. Differences in the quantity of opaline silicaoccur between species and between parts of the same species.The amount of opal deposited in the soil annually by root systemsand above-ground parts is approximately equal in magnitud Andropogon gerardi, Sorgastrum nutans, Panicum virgatum, opaline silica deposition     

A correlated light and electron microscopic study of the structure and secretory activity of the accessory salivary glands of the marine gastropods,Conus flavidus and C. vexillum (neogastropoda,conacea)

The structure and secretory activity of the accessory salivary gland in two species of Conus were examined using routine and histochemical techniques of light, scanning and transmission electron microscopy. The composite layers of the accessory salivary gland of Conus are a luminal epithelium, fibromuscular layer, submuscular layer, and a capsule. In C. flavidus and C. vexillum, the luminal epithelium is formed by epitheliocytes and cytoplasmic processes extending from the secretory cells, whose perikarya form the submuscular layer. The processes carry secretory cell products (chiefly Golgi-derived glycoprotein) across the fibromuscular layer and terminate between epitheliocytes (at the bases of the secretory canaliculi) or beyond the surface of the epithelial cells. Conus vexillum is distinguished from C. flavidus by its high content of lipofuscin. Epitheliocytes are the only microvillated cells in the accessory salivary gland of Conus. In C. flavidus, epitheliocytes extrude secretory granules, various types of cytoplasmic blebs and clear vesicles by apocrine “pinching off”. Clear vesicles are shed from the tips of microvilli. The luminal epithelial cells of C. vexillum similarly egest clear vesicles, but normally undergo additional holocrine secretion to release lipofuscin. The secretions of epitheliocytes appear to be major products of the accessory salivary gland: consideration of secretory activities by both epitheliocytes and secretory cells will therefore be necessary when directly investigating accessory salivary gland function in Conus.     

小地老虎雄蛾中胚层生殖道和附腺的细胞结构和分泌功能

通过光镜、电镜及组织化学等方法,研究了小地老虎生殖前期雄蛾中胚层生殖道和附腺的腺细胞结构和分泌功能,以及与精子形态和数量变化的关系,结果表明：(1)以缢缩位置、解剖形态、细胞结构、分泌方式、精子形态变化和数量变动为依据,将中胚层生殖道划分为修精囊、输精管、贮精囊、精包腺1～5段等8个区段;(2)中胚层生殖道和附腺具有相同的组织层次,自内向外分为单细胞上皮层、底膜、肌肉层和围膜等4层,但缺少表皮质内膜;(3)中胚层生殖道和附腺的腺细胞具有旺盛的合成和分泌蛋白质的能力,主要有内质网型和液泡型两种,前者有发达的粗面内质网和高尔基体,后者具有致密的核糖体和分泌泡;至少有4种分泌方式：即颗粒顶泌、液泡顶泌、胞质局泌和胞间分泌;修精囊、贮精囊、雄性附腺、精包腺1段的顶泌物为糖蛋白性质(PAS阳性)、局泌物为非糖蛋白性质(PAS阴性)。     

Excitatory Transmission in Insect Neuromuscular Systems

Many, but not all, visceral muscles in insects are innervatedby neurosecretory axons. The neurosecretory junctions with theheart muscle of the American cockroach, Periplaneta americana,show ultrastructural and electrophysiological evidence of chemicallytransmitting synapses, and cytochemical evidence for the presenceof monoamines. Electron microscopy of nerve terminals showsthat synaptic vesicles may be formed directly from electron-dense"neurosecretory" granules Neurotomy of motor axons to skeletal muscles in insects leadsto aggregation and clumping of synaptic vesicles after 48 hours.Treatment of in vitro nerve-muscle preparations with variousrespiratory poisons caused aggregation similar to that developedin neurotomized animals. This suggested that vesicle aggregationin both cases may have resulted from a decrease in availableadenosine triphosphate in the nerve terminal with subsequentalteration in the normal charge density which supports a repulsiveforce between the vesicles.     

The light organ and ink sac of Heteroteuthis dispar (Mollusca: Cephalopoda)

There has previously been some dispute over the source of the light of Heteroteuthis. Light and electron microscopy have shown that there are no bacteria in the cavity of the luminous gland, but rather a population of spherical vesicles of varying size and content, surrounded by dense interstitial material. The contents are secreted by the cells surrounding the gland via a microvillous brush border that contains cilia. The gland is surrounded by a reflector layer made up of iridophores, whose structure differs considerably in the proximal, lateral and cap regions.
The ink sac contains masses of spherical dense granules and its wall cells have many microvilli extending amongst these granules.     

Fine structure of the accessory glands of the female genital tract of the ichneumonid Pimpla turionellae (Insecta,Hymenoptera)

Summary The female accessory glands include the tubular poison gland, the paired, lemon-shaped uterus glands, and Dufour's gland, an unbranched tubular organ. They consist essentially of a single layer of epithelium cells surrounded by a basement membrane. The lumen is lined by cuticle. The proteinaceous secretion of the poison gland is released into intracellular ducts provided with microvilli, each connected to a channel lined with cuticle which leads to the central lumen of the gland. The channel is formed by special canal cells. Nerve endings are interspersed among the gland cells. The uterus gland consists of four cell types derived from a single type of precursor cell found in newly hatched wasps. Type I cells are covered by type II cells and are thus without contact to the luminal surface of the gland. They contain stacks or whorls of mitochondria and smooth cisternae in an alternating arrangement. Vesicles with a secretory product are found in cells of types II and III. Deep anastomosing infoldings of the plasmalemma, stabilized by microtubules and dense material at the branchings, are characteristic for type II cells. Most secretory vesicles are found in type III cells, the prevalent cell type which is thought to be the source of the lipoprotein secretion. Coated vesicles are present at deep infoldings of the plasmalemma. The greatly enlarged apical surface area of type IV cells and the presence of mitochondria in slender outgrowths is suggestive of an osmoregulatory function. In Dufour's gland, two cell types appear in succession, the first with a very dense cytoplasm, the second with dense inclusions and many seemingly empty vesicles of smooth endoplasmic reticulum. The secretion products, lecithin and a cholesterol ester, are thought to be formed by the second cell type. The dense inclusion might be lecithin, which reacts with osmium tetroxide. The cholesterol ester could have been washed out of the empty vesicles by the embedding procedure.     

Ultrastructural Changes Associated with Spore Formation in Sporangia and Sporangiola of Thamnidium elegans Link

Fully formed pre-cleavage sporangia and sporangiola of Thamnidiumelegans Link were bounded by a primary wall plus a thick, internalsecondary wall layer. In sporangia in late pre-cleavage, Golgi-likecisternae were associated with groups of cytoplasmic vesiclesof characteristic size and appearance which were not found insporangia containing large cleavage vesicles. In both sporangia and sporangiola, protoplast cleavage was effectedby enlargement of endogenous cleavage vesicles each containinga lining layer of variable appearance, mutual fusion of cleavagevesicle membranes and fusion of cleavage vesicle membranes withthe plasmalemma. Golgi-like cisternae and small vesicular profileswere present in sporangium protoplasts at all stages of cleavagevesicle enlargement. In sporangia, the columella zone was delimitedby cleavage vesicles and separated from the sporogenous zoneby a fibrillar wall. A similar wall, which sometimes protrudedto form a small columella, was formed in sporangiola. Recently delimited spore protoplasts were bounded by plasmalemmamembrane derived from cleavage vesicle bounding membrane andsporangium or sporangiolum plasmalemma and surrounded by aninvesting layer derived from cleavage vesicle lining material.The investing layer at first appeared single, but later twoelectron opaque profiles were discernible. The spore wall wasformed between the investing layer and the plasmalemma. Wallsof sporangia and sporangiola which contained fully formed sporesconsisted of the primary layers only.     

Mechanics of curved plasma membrane vesicles: resting shapes, membrane curvature, and in-plane shear elasticity

Highly curved cell membrane structures, such as plasmalemmal vesicles (caveolae) and clathrin-coated pits, facilitate many cell functions, including the clustering of membrane receptors and transport of specific extracellular macromolecules by endothelial cells. These structures are subject to large mechanical deformations when the plasma membrane is stretched and subject to a change of its curvature. To enhance our understanding of plasmalemmal vesicles we need to improve the understanding of the mechanics in regions of high membrane curvatures. We examine here, theoretically, the shapes of plasmalemmal vesicles assuming that they consist of three membrane domains: an inner domain with high curvature, an outer domain with moderate curvature, and an outermost flat domain, all in the unstressed state. We assume the membrane properties are the same in these domains with membrane bending elasticity as well as in-plane shear elasticity. Special emphasis is placed on the effects of membrane curvature and in-plane shear elasticity on the mechanics of vesicle during unfolding by application of membrane tension. The vesicle shapes were computed by minimization of bending and in-plane shear strain energy. Mechanically stable vesicles were identified with characteristic membrane necks. Upon stretch of the membrane, the vesicle necks disappeared relatively abruptly leading to membrane shapes that consist of curved indentations. While the resting shape of vesicles is predominantly affected by the membrane spontaneous curvatures, the membrane shear elasticity (for a range of values recorded in the red cell membrane) makes a significant contribution as the vesicle is subject to stretch and unfolding. The membrane tension required to unfold the vesicle is sensitive with respect to its shape, especially as the vesicle becomes fully unfolded and approaches a relative flat shape.     

Ultrastructure of copulatory organs in Turbellaria

Summary The copulatory organs in Macrostomum sp. and Microstomum sp. contain simple tubular stylets which are intracellular specializations. The stylet in Macrostomum sp. is produced in a syncytium covering part of the prostatic vesicle. The proximal region of the stylet surrounds the vesicle which contains six prostatic gland ducts and six accessory (sensory) cells containing ciliary rootlets. The stylet in Microstomum sp. is produced in an extension of a syncytium which lines the combined seminal-prostatic vesicle. The stylet is connected to the combined vesicle by a narrow bridge of matrix syncytium through which sperm, prostatic gland products and sensory cilia pass from the vesicle to the stylet lumen. In both species the matrix syncytium can be interpreted as a specialized terminal end of the male canal epithelium. Stylets of Turbellaria and other lower Metazoa are discussed in regards to structure (one or several pieces) and location (in separate cells, in a syncytium, or extracellular).Abbreviations used in figures ac accessory cell - b basal body - c cilium - cv combined vesicle - d prostatic gland duct - dc degenerative cell - di dictyosome - e epidermis - ed ejaculatory duct - g prostatic gland cell - h hemidesmosome - i intercellular matrix - im internal muscle - in intestine; - l lumen of male canal - lm longitudinal muscle - m matrix syncytium - mc male canal epithelial cell - mi microfilaments - mt microtubules - mu muscle cell - mv microvilli - n nucleus - np nerve process - ns neurosecretory (?) granule - p prostatic vesicle - pv prostatic part of combined vesicle - r rootlet - s stylet - sm stylet material - sp sperm - sv seminal part of combined vesicle     

The Ultrastructure of the Digestive Glands in Pinguicula vulgaris L. (Lentibulariaceae) Relative to their Function. I. The Changes During Maturation

The digestive glands of Pinguicula vulgaris become fully maturewhilst still enclosed in the bud. All the gland cells remainintact on the fully expanded unstimulated leaves. As the secretoryhead cells mature, a special layer forms between the plasmalemmaand the cell wall. This layer is shown to be different fromthe typical labyrinthine wall of transfer cells and serves forthe storage of digestive enzymes. Ultrastructural analysis,including morphometry, indicates that the digestive enzymesare synthesized on the RER of the head cells and transferredinto the cell wall, particularly into the slime layer, and vacuoles.This transfer is achieved firstly through continuity of theendoplasmic reticulum with vacuoles (static) and the periplasmicspace (dynamic) and, secondly, into the latter through exocytosisof coated Golgi vesicles and of some vacuoles filled with enzymes. Pinguicula vulgaris L., carnivorous plant, digestive glands, ultrastructure, protein synthesis secretion     

Pollination and Pollen-pistil Interaction in Oil Palm, Elaeis guineensis

Structural and cytochemical aspects of the pistil and detailsof pollination and pollen-pistil interaction were investigatedin the African oil palm (Elaeis guineensis Jacq.), an importantperennial oil crop. The stigma is trilobed, wet and papillate.The branched papillae are confined to a narrow linear zone oneach stigmatic lobe. Each stigmatic lobe harbours a deep stigmaticgroove, which runs adaxially along the surface. The stigmaticgroove is bordered by a well-defined layer of glandular cells,each of which has a pectinaceous cap on the inner tangentialwall. The style is hollow. The canal cells show thickeningson the inner tangential wall. The stigmatic groove and stylarcanal contain an extracellular matrix secreted by the canalcells which is rich in proteins, acidic polysaccharides andpectins. The canal cells at the base of the style are papillateand loosely fill the stylar canal. The stigma becomes receptivewhen the stigmatic lobes separate, and remains so for 24 h.Pollination is mediated by weevils as well as by the wind. Undernatural conditions the pollination efficiency was 100%. Pollinationinduces additional secretion in the stigmatic groove and stylarcanal. During post-pollination secretion, the pectinaceous capsof the cells lining the stigmatic groove are degraded. Pollengrains germinate on the stigmatic papillae and tubes grow onthe surface of the papillae, entering the stigmatic groove andadvancing along it into the stylar canal to eventually gainaccess to the locules. Pollen tubes are seen in the ovules 18–20h after pollination. Copyright 2001 Annals of Botany Company Arecaceae, Elaeis guineensis, African oil palm, pollination, stigmatic grove, stylar canal, Tenera hybrid, weevil