MORPHOLOGY,SEASONAL VARIATION,AND FUNCTION OF RESIN GLANDS ON BUDS AND LEAVES OF POPULUS DELTOIDES (SALICACEAE)

When buds form in summer or early fall, modified stipules act as bud scales and their adaxial epidermis secretes a resin that fills the bud. This secretory layer collapses in the dormant bud. Immature leaves, stipules, and leaf primordia occupy the center of the bud; all lack functional resin glands. In spring, stipules of emerging leaves develop an adaxial palisadelike secretory epidermis that becomes more ridged longitudinally in successive stipules. Marginal teeth of the first leaves to emerge are covered with trichomes and lack a secretory epidermis. In successive leaves the teeth become glandular and secrete resin as the lamina unrolls. Later in the season, marginal leaf glands account for much of the resin. Unspecialized hydathodes or extrafloral nectaries occur proximal to each glandular tip. Guttation of water or nectar occurs here through stomata located above a vein ending. On the basis of field observations and a laboratory feeding experiment, the resin seems to function mainly as an insect repellent. It may also reduce water loss from young leaves.     

MORPHOLOGY AND ANATOMY OF RESIN GLANDS IN SALIX LUCIDA (SALICACEAE)

Resin glands on the first leaves to emerge occur at the tip of each marginal dentation of the lamina and stipule, and on the adaxial surface of the stipule and lamina bases (the latter often extend onto the petiole). Successive emerging leaves show increases in number of basilaminar glands, because increasingly elaborate multiglandular stalks develop. Glands in all locations are conical or domed, with a palisade-like epidermis subtended by 5–6 layers of parenchyma which contains druse crystals. A single vascular bundle (sometimes two or three) ends in a small knob of tracheary elements. Glands usually secrete liquid resin that covers the gland and surrounding area and under certain conditions, particularly in low humidity, resin is extruded as a filament from a pore in the gland apex, a mode of resin secretion not described previously. Glands secreting liquid resin have an apical dimple, but presence of a pore has not been established.     

Floral nectar production and carbohydrate composition and the structure of receptacular nectaries in the invasive plant <Emphasis Type="Italic">Bunias orientalis</Emphasis> L. (Brassicaceae)

The data relating to the nectaries and nectar secretion in invasive Brassicacean taxa are scarce. In the present paper, the nectar production and nectar carbohydrate composition as well as the morphology, anatomy and ultrastructure of the floral nectaries in Bunias orientalis were investigated. Nectary glands were examined using light, fluorescence, scanning electron and transmission electron microscopy. The quantities of nectar produced by flowers and total sugar mass in nectar were relatively low. Total nectar carbohydrate production per 10 flowers averaged 0.3 mg. Nectar contained exclusively glucose (G) and fructose (F) with overall G/F ratio greater than 1. The flowers of B. orientalis have four nectaries placed at the base of the ovary. The nectarium is intermediate between two nectary types: the lateral and median nectary type (lateral and median glands stay separated) and the annular nectary type (both nectaries are united into one). Both pairs of glands represent photosynthetic type and consist of epidermis and glandular tissue. However, they differ in their shape, size, secretory activity, dimensions of epidermal and parenchyma cells, thickness of secretory parenchyma, phloem supply, presence of modified stomata and cuticle ornamentation. The cells of nectaries contain dense cytoplasm, plastids with starch grains and numerous mitochondria. Companion cells of phloem lack cell wall ingrowths. The ultrastructure of secretory cells indicates an eccrine mechanism of secretion. Nectar is exuded throughout modified stomata.     

FOSSIL EXTRAFLORAL NECTARIES,EVIDENCE FOR THE ANT-GUARD ANTIHERBIVORE DEFENSE IN AN OLIGOCENE POPULUS

Extrafloral nectaries are secretory glands, usually found on leaves, that have been shown to promote ant defense against the insect herbivores of many modem day plants. Extrafloral nectaries were found on the 35-million-year-old fossil leaves of the extinct Populus crassa from Florissant, Colorado. Extinct ant species (belonging to five still extant genera that have modem ant-guard species), and other predators and parasitoids (whose modem relatives frequent extrafloral nectaries) also lived at Florissant. The extrafloral nectaries of P. crassa (and perhaps other plants) probably operated to attract ants and/or other arthropod defenders as early as the Oligocene.     

Chloroplast-ultrastructure and chlorophyll content in leaves from Quercus branches with and without epiphytic lichen thalli

Abstract The effect that the massive presence of lichen thalli growing on the branches of Quercus pyrenaica and Q. rotundifolia leaves has on their chloroplasts been studied. In both species there were significant decreases in the amount of chlorophylls in the leaves of twigs with a dense cover of lichens in comparison with the leaves from thallus-free twigs. The areas and perimeter of chloroplasts in leaves from twigs with epiphytes did not differ significantly from those in leaves without epiphytes. However, in leaves with epiphytes the percentage of chloroplast area occupied by starch was higher. In Q. pyrenaica the number of grana per chloroplast section and per μm², the percentage of chloroplast stroma occupied by grana, the average number of thylakoids forming grana and the grana width was significantly smaller in leaves near lichen populations. These results are discussed and related to the great chelating capacity of the lichen's substances.     

Anatomical and histochemical characterization of extrafloral nectaries of Prockia crucis (Salicaceae)

Besides being vital tools in taxonomic evaluation, the anatomy of plant secretory structures and the chemical composition of their secretions may contribute to a more thorough understanding of the roles and functions of these secretory structures. Here we used standard techniques for plant anatomy and histochemistry to examine secretory structures on leaves at different stages of development of Prockia crucis, to evaluate the origin and development of the structures, and to identify the disaccharides and monosaccharides in the exudates. Fructose, glucose, and sucrose constituted up to 49.6% of the entire secretion. The glands were confirmed to be extrafloral nectaries (EFNs); this is the first report of their presence in the genus Prockia. These EFNs are globular, sessile glands, with a central concavity occurring on the basal and marginal regions of the leaf. The epidermis surrounding the concavity is secretory, forming a single-layered palisade that strongly reacts with periodic acid-Schiff's reagent (PAS) and xylidine Ponceau, indicators of total polysaccharides and total proteins, respectively, in the exudate. On the basis of the similarity of these glands to the salicoid teeth in Populus and Salix, we suggest that these three taxa are phylogenetically close.     

A flower with several secretions: anatomy,secretion composition,and functional aspects of the floral secretory structures of Chelonanthus viridiflorus (Helieae—Gentianaceae)

Floral secretory structures have been reported for Gentianaceae; however, morphoanatomical studies of these glands are rare. We described the development and secretory activity of the colleters and nectaries throughout the floral development of Chelonanthus viridiflorus. We collected flower buds, flowers at anthesis, and fruits to be investigated using light and scanning electron microscopy. We performed histochemical tests on the secretion of colleters and used glycophyte to confirm the presence of glucose in nectar. Colleters are located on the ventral surface of sepals and nectaries occur in four regions: (i) the dorsal and (ii) ventral surfaces of sepals; (iii) apex of petals; and (iv) base of ovary. The colleters have a short peduncle and a secretory portion with homogeneous cells. They are active in flower buds and secrete polysaccharides and proteins. In flowers at anthesis, they begin to senescence presenting protoplast retraction, cell collapse, and lignification; these characteristics are intensified in fruit. The nectaries of sepals and petals have two to five cells surrounding a central cell through which the secretion is released. Nectaries are numerous, forming a nectariferous area on the dorsal surface of sepals, like that observed on petals, and can form isolated units on the ventral surface of sepals. They are active from flower buds to fruits. A region with secretory activity was identified at the base of the ovary. The secretion of colleters acts in the protection of developing organs, while nectaries are related to defenses against herbivores and the supply of nectar to potential robbers or pollinators.

     

Structure and development of bracteal nectary glands in Aphelandra (Acanthaceae)

A survey of bracteal (extrafloral) nectaries in species of Aphelandra (Acanthaceae) reveals substantial diversity. Each bracteal nectary is an aggregate of individual glands that vary in number, size, and structure among species. Glands contain three cell layers: a palisade-like secretory cell layer, a one-to-many-celled intermediate layer with thickened cell walls, and a foot layer. Members of the A. pulcherrima complex have one of two distinct gland types: relatively small glands with a single-celled intermediate layer or larger glands that have a multicellular intermediate layer. Nectaries composed of small glands are patches of many (>50) glands, whereas those composed of large glands are patches of < 10 glands. Four outgroup species have bracteal nectaries of numerous small glands with pluricellular intermediate layers. Glands of all three types are initiated as single enlarged protodermal cells, and all undergo similar early periclinal divisions; the large-gland type shows greater subsequent enlargement with many more anticlinal divisions. The bracteal nectar glands are interpreted to be homologous with simpler glandular trichomes, and mark a monophyletic lineage within Aphelandra. Comparisons with outgroup species show that both nectary types in the A. pulcherrima complex have diverged from an ancestral condition of numerous small glands with pluricellular intermediate layers. Use of the ontogenetic criterion to polarize gland type within the A. pulcherrima complex would yield erroneous results because evolution has apparently involved a developmental truncation with loss of cell divisions in the intermediate layer of small glands. Comparable nectar glands in more distant taxa are interpreted as remarkable cases of convergent evolution, perhaps from similar trichome precursors.     

STEMS AND LEAVES OF CUNNINGHAMIOSTROBUS GOEDERTII FROM THE OLIGOCENE OF WASHINGTON

This report is based on nine specimens of fossil conifer stems and leaves from the Early Oligocene Jansen Creek Member of the Makah Formation. They were collected along the northern shore of the Olympic Peninsula of Washington. The fossils are preserved as siliceous permineralizations and were exposed in surface view along rock fractures. Details of leaf morphology and epidermal construction appear on fracture surfaces of certain specimens while the cellular construction of the leaves and twigs is visible in thin sections. Leaves are dorsiventrally flattened, attached to twigs that contain up to four growth increments of secondary xylem, up to 2.3 cm long, 3.5 mm wide, and have parallel margins with minute teeth. The leaves are about 0.5 mm thick and have a central vascular strand surrounded by transfusion tissue. A large resin canal occurs abaxial to the vascular strand, and generally two additional resin canals occur in the mesophyll near each leaf margin. Leaves are mostly hypostomatic, with sunken stomata in two longitudinal bands, one to each side of the midline of the leaf and each containing eight to 13 longitudinal rows of stomata. Several unusual anatomical features in the stems also occur in the peduncle and cone axis of seed cones described as Cunninghamiostrobus goedertii, which occurs at the same locality. Thus, the leafy twigs belong to the same species as produced the cones. The cones, leaves, and shoots of this Tertiary conifer are similar to those of modern Cunninghamia but differ from the living species in several respects.     

Morpho–anatomical and ultrastructural analysis of extrafloral nectaries in Inga edulis (Vell.) Mart. (Leguminosae)

The presence of extrafloral nectaries (EFNs) between leaflets is an usual feature in Inga edulis (Vell.) Mart. (Leguminosae). Extrafloral nectaries are secretory structures involved in production of nectar and which serve in the protection of plants against herbivores through association with ants. This study aimed to characterize the EFNs of I. edulis at different developmental stages and describe their morphology, histochemistry and ultrastructure. Leaf fragments, containing secretory structures, were processed according to standard methods for light, scanning and transmission electron microscopy. The EFNs were classified into three stages based on morphology: pre‐secretory, secretory and post‐secretory. The pre‐secretory stage occurs in young leaves, whereas secretory and post‐secretory stages occur in developed and senescent leaves, respectively. The EFNs possess a concave surface and a central cleft in which nectar is accumulated and which was not observed in pre‐secretory EFNs. Histochemical tests identified the presence of sugars, proteins, phenolic compounds, mucilage and lipids at all developmental stages of the EFNs. Calcium crystals were identified in all tissues and stages of the EFNs. The secretory cells of the EFNs exhibit a granular cytoplasm, small vacuoles, prominent nuclei, smooth endoplasmic reticulum and mitochondria. Post‐secretory stage EFNs exhibited intense cytoplasmic degradation and the presence of microorganisms. The performance of EFNs of I. edulis appear to follow the leaf development.     

LEAF DIMORPHISM IN POPULUS TRICHOCARPA

Critchfield , William B. (Pacific SW Forest & Range Expt. Sta., Berkeley, Calif.) Leaf dimorphism in Populus trichocarpa. Amer. Jour. Bot. 47 (8) : 699–711. Illus. 1960.—In Populus trichocarpa and other species of Populus, each tree bears 2 kinds of leaves, referred to here as “early” and “late” leaves. Both leaf types are present on all long shoots. They differ in many features of external morphology, including petiole length, size and occurrence of marginal glands, venation, and stomatal distribution. This type of foliar dimorphism has its origins in a pronounced difference in leaf ontogeny. The early leaves originate in the developing bud and overwinter as embryonic leaves. The first late leaves are also present in the winter bud, but as arrested primordia, and succeeding late leaves are initiated at the tip of the growing shoot and develop uninterruptedly to maturity during the growing season. A similar correlation between leaf form and the circumstances of leaf ontogeny appears to be a common feature of many other instances of heterophylly. The expansion of the pre-formed early leaves is almost completed by late spring, when the first late leaves begin to grow rapidly. The formation of late leaves may then continue until late in the season. The rapid elongation of the stem does not begin until the first late leaves expand. Elongation is restricted to shoots producing late leaves. Consequently, the early leaves are confined to short shoots and the base of long shoots; adventitious shoots and the upper part of long shoots bear only late leaves. Certain other woody plants with long and short shoots also exhibit a restriction of elongation to those shoots on which a second set of leaves is produced.     

Ultrastructure of epidermal glands in neotenic reproductives of the termite Prorhinotermes simplex (Isoptera: Rhinotermitidae)

The ultrastructure of epidermal glands in neotenic reproductives of Prorhinotermes simplex is described and their development is compared among young and old neotenics of both sexes. Secretory cells forming the epidermal gland are attached to the cuticle all over the body. The glands are formed by class 1 and class 3 secretory cells and corresponding canal cells with secretory function. Class 1 cells are sandglass-like and class 3 secretory units are located among them. Class 1 cells contain predominantly tubular endoplasmic reticulum, the major part represents the smooth and the minor the rough form. Numerous electron dense granules occur in the cytoplasm, they are always disintegrated prior to be released. Class 3 secretory cells contain a large amount of vacuoles, which are always lucent in males while newly produced vacuoles are dense in females. Dense vacuoles are frequently transformed into lucent ones before being released. Canal cells are locally equipped with microvilli. The conducting canal is surrounded by an electron dense secretion of regular inner structure. The cytoplasm of the canal cell contains numerous mitochondria, rough endoplasmic reticulum and a large proportion of microtubules. The young neotenic reproductives differ from the old ones by a lower amount of secretory products. Epidermal glands probably produce substances inhibiting the occurrence of superfluous reproductives.     

Peptide secretion in the cutaneous glands of South American tree frog Phyllomedusa bicolor: an ultrastructural study

The development of the dermal glands of the arboreal frog Phyllomedusa bicolor was investigated by immunocytochemistry and electron microscopy. The 3 types of glands (mucous, lipid and serous) differed in size and secretory activity. The mucous and serous glands were apparent in the tadpole skin, whereas the lipid glands developed later in ontogenesis. The peptide antibiotics dermaseptins and the D-amino acid-containing peptide opioids dermorphins and deltorphins are abundant in the skin secretions of P. bicolor. Although these peptides differ in their structure and activity they are derived from precursors that have very similar preproregions. We used an antibody to the common preproregion of preprodermaseptins and preprodeltorphins and immunofluorescence analysis to show that only the serous glands are specifically involved in the biosynthesis and secretion of dermaseptins and deltorphins. Scanning and transmission electron microscopy revealed that the serous glands of P bicolor have morphological features, especially the secretory granules, which differ from those of the glands in Xenopus laevis skin.     

Studies in the secretory glands of Hiptage sericea (Malpighiaceae)

Hiptage sericea is shown to possess both lipophilic glands and extrafloral nectaries. Both types of glands develop from a group of initials and show similarities in organisation of tissue systems and secretion. The nature of the secretory substances is however different. The occurrence and function of the glands are discussed.     

荇菜花蜜腺的发育研究

荇菜花蜜腺的发育过程可分为：起源期、生长期、分泌期以及泌蜜停止期等４个时期。荇菜的５枚花蜜腺均起源于子房基部的表皮及表皮内的２－４层细胞。这些细胞经反分化后分别成为蜜腺的原分泌表皮及原泌蜜组织,两部分细胞径不断地分裂分化,最冬成为成熟蜜腺。在蜜腺发育过程中,蜜腺的分泌表皮及蜜腺组织内的内质网、质体、线粒体、液泡等细胞器结构均发生了有规律的变化,内质网在蜜腺分泌期最为发达,且产生大量的分泌小泡。质体     

Anatomy and histochemistry of the nectaries of Rodriguezia venusta (Lindl.) Rchb. f. (Orchidaceae)

Orchidaceae is one of the largest angiosperm families. Although extensively studied, reports of anatomy of secretory structures of orchids are relatively scarce. Rodriguezia venusta is an epiphytic orchid occurring in Brazil and Peru that has floral and extrafloral nectaries. This study describes the structure and the histochemistry of these secretory structures. Floral and extrafloral nectary samples were obtained from R. venusta plants that were collected in a gallery forest in the State of Bahia, Brazil, and grown in a greenhouse. Theses samples were fixed and processed according to routine procedures in plant anatomy and histochemistry or for scanning electron microscopy. The extrafloral nectaries occur on the edge and sub-edge of young leaves and at the basal portion of bracts that subtend the floral buds. They are structurally very similar, being formed by a nectary parenchyma and a simple epidermis with stomata (“non-structured nectaries”). The floral nectary is inserted at the floral receptacle fused with the labellum base, between this structure and the two inferior connate sepals. This nectary consists of an epidermis with numerous specific nectar secreting trichomes, a subnectary and a nectary parenchyma abundantly supplied by vascular terminations. Its structure is complex and distinct from other floral nectaries described for Orchidaceae.     

Programmed cell death during pigment gland formation in Gossypium hirsutum leaves

Ultrastructural studies have shown that the formation of pigment glands in Gossypium hirsutum L. leaves is a lysigenous process, originating from a cluster of cells in the ground meristem. Various techniques were used here to investigate whether programmed cell death (PCD) plays a critical role in this developmental process. Nuclei of internal cells in the pigment gland‐forming tissue were TUNEL‐positive and DAPI‐negative, suggesting that DNA cleavage is an early event and complete DNA degradation is a late event. Smeared bands and a lack of laddering after gel electrophoresis indicate that DNA cleavage is random. Ultrastructurally, secretory cells in the pigment glands become distorted, nuclei are densely stained, and chromosomes become condensed until completely degraded at late stages. Vacuoles with electron‐dense bodies and membrane‐bound autophagosomes are seen in both secretory and sheath cells, suggesting that autophagy plays a key role in PCD during cytoplasm degradation. Buckling of cell walls, seen at early stages, later leads to a complete breakdown of the walls. Together, these results suggest that PCD plays a critical role in the lysigenous development of pigment glands in G. hirsutum leaves.     

Morphology, development and homologies of the perianth and floral nectaries in Croton and Astraea (Euphorbiaceae-Malpighiales)

New observations are presented on the ontogeny, vasculature and morphology of both staminate and pistillate flowers of Croton and Astraea. These data support earlier hypotheses that the filamentous structures in pistillate flowers represent reduced and transformed petals. Staminate flowers of both genera possess five free nectaries, which are vascularised by divergences of the sepal traces in Croton and unvascularised in Astraea. In pistillate flowers, there are five separate non-vascularised nectaries in Astraea, but in Croton there is a single nectariferous disk that is vascularised by divergences of the sepal traces. The nectaries are initiated late in floral development, but their location indicates that they could represent the outer stamen whorl transformed into secretory staminodes. Other glandular structures occur in pistillate flowers of most Croton species, resulting in flowers with two secretory organ whorls. In these cases, the inner whorl is formed by modified staminodes. Our observations support the recent segregation of Astraea species from the larger genus Croton. Despite strong similarities between the two genera, there are clear structural differences, including the presence of colleters in Astraea (absent in Croton), moniliform trichomes on petals (rather than simple trichomes in Croton), non-vascularised nectaries (vascularised in Croton) and reduced, non-secretory filamentous structures (well developed and secretory in Croton).     

Stimulation of fibroin synthesis elicits ultrastructural modifications in spider silk secretory cells

Electron microscopic studies of unstimulated and stimulated spider fibroin glands show that the fibroin synthesis stimulus evokes visible changes in both the endoplasmic reticulum and Golgi apparatus of their secretory epithelium. Gradual increase in distension of the reticulum accompanies the increase of evoked fibroin synthetic activity. The flattened translucent Golgi vesicles, seen in inactive cells, display a gradual increase in size and number, also with time. The stimulation also elicits a gradual transition in the gland's luminal membrane, during which the microvilli on the lining gradually disappear acquiring an electron dense appearance. Correlations of the observed transitions to the gland's increase in rate of elicited synthetic activity are discussed. The parallelisms between the ultrastructural modifications observed in the spider secretory cells with those described in the silkworm glands during their progression through the fifth instar have been stressed.