Melanin deposits associated with the venom glands of snakes

Melanin deposits in the heads of both true vipers (Viperinae) and pit vipers (Crotalinae) are concentrated over the dorsal and dorsolateral aspects of the venom glands. This pigment may occur in any or all of six sites which include the epidermis, dermis, tissues covering the venom glands, and the interior of the glands themselves. The extreme localization of these melanin deposits suggests that they shield the venom glands from light. Calculations indicate that without such shielding the light energy penetrating the venom glands in the visible and ultraviolet portions of the solar spectrum would damage the venom-synthesizing apparatus and detoxify stored venom. Elapid and hydrophiid snakes have less dense pigment over the venom gland than vipers. Literature reports indicate that elapid venom is less sensitive to photodetoxification than is venom from vipers. Most colubrid snakes, including several with protein-secreting Duvernoy's glands, have little or no melanin associated with the glands. Venomous colubrids in the genera Ahaetulla, Dryophis, Leptophis, and Oxybelis have pigment over the glands as dense as that seen in vipers. Iridophores probably also shield venom glands from radiation. In puff adders and Gaboon vipers (Bitis) there appears to be an ontogenetic change in the shielding of the venom glands from melanocytes in young individuals to iridophores in adults.     

Bar synapses in the end buds of lamprey skin

Summary The end buds of lamprey epidermis have been considered to be similar to taste buds, but the synapses on the receptor cells are of the type with a dense mass surrounded by lucent vesicles, which is not found in gustatory cells. It is suggested that the end buds may belong to the lateralis sensory system and be involved in the light sensitivity of lamprey skin.     

An ultrastructural study of the prostate gland of megascolicid earthworm Lampito mauritii (Kinberg)

The ultrastructure of prostate gland of Lampito mauritii revealed two types of secretory cells. Type 1 cells with a broad basal region and a long apical region contain electron dense oval secretory granules with an increased density at the core region. Numerous electron lucent granules with fine filamentous and electron dense amorphous materials also occur at the basal region of these cells. Type 2 cells contain electron lucent mucous-like secretory granules. This cell type contains exceptionally large Golgi complexes having 20-23 stacked cisternae. Both cell types open into a common lumen and numerous microtubules are visible at the apical end. Junctional complexes, such as desmosomes and septate junctions, are observed in this glandular tissue.     

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.     

Seed coat development, anatomy and scanning electron microscopy of Harpagophytum procumbens (Devil's Claw), Pedaliaceae

Seed coat development of Harpagophytum procumbens (Devil's Claw) and the possible role of the mature seed coat in seed dormancy were studied by light microscopy (LM), transmission electron microscopy (TEM) and environmental scanning electron microscopy (ESEM). Very young ovules of H. procumbens have a single thick integument consisting of densely packed thin-walled parenchyma cells that are uniform in shape and size. During later developmental stages the parenchyma cells differentiate into 4 different zones. Zone 1 is the multi-layered inner epidermis of the single integument that eventually develops into a tough impenetrable covering that tightly encloses the embryo. The inner epidermis is delineated on the inside by a few layers of collapsed remnant endosperm cell wall layers and on the outside by remnant cell wall layers of zone 2, also called the middle layer. Together with the inner epidermis these remnant cell wall layers from collapsed cells may contribute towards seed coat impermeability. Zone 2 underneath the inner epidermis consists of large thin-walled parenchyma cells. Zone 3 is the sub-epidermal layers underneath the outer epidermis referred to as a hypodermis and zone 4 is the single outer seed coat epidermal layer. Both zones 3 and 4 develop unusual secondary wall thickenings. The primary cell walls of the outer epidermis and hypodermis disintegrated during the final stages of seed maturation, leaving only a scaffold of these secondary cell wall thickenings. In the mature seed coat the outer fibrillar seed coat consists of the outer epidermis and hypodermis and separates easily to reveal the dense, smooth inner epidermis of the seed coat. Outer epidermal and hypodermal wall thickenings develop over primary pit fields and arise from the deposition of secondary cell wall material in the form of alternative electron dense and electron lucent layers. ESEM studies showed that the outer epidermal and hypodermal seed coat layers are exceptionally hygroscopic. At 100% relative humidity within the ESEM chamber, drops of water readily condense on the seed surface and react in various ways with the seed coat components, resulting in the swelling and expansion of the wall thickenings. The flexible fibrous outer seed coat epidermis and hypodermis may enhance soil seed contact and retention of water, while the inner seed coat epidermis maintains structural and perhaps chemical seed dormancy due to the possible presence of inhibitors.     

Designer skin: lineage commitment in postnatal epidermis

The epidermis is populated by stem cells that produce daughters that differentiate to form the interfollicular epidermis, hair follicles and sebaceous glands. Diffusible factors, cell-cell contact and extracellular matrix proteins are all important components of the microenvironment of individual stem cells and profoundly affect the differentiation pathways selected by their progeny. Here, we summarize what is known about stem-cell populations and lineage relationships within the epidermis. We also present evidence that postnatal epidermis can be reprogrammed, altering the number and location of cells that differentiate along specific epidermal lineages.     

Ultrastructural identification of the antennal gland complement in Siagona europaea Dejean 1826, a myrmecophagous carabid beetle

We examined antennal exocrine glands in adults of a myrmecophagous carabid beetle, Siagona europaea Dejean 1826 (Coleoptera, Carabidae), by light and electron microscopy and we identified two types of integumentary glands. The first type includes glands formed by three cells (a secretory cell, an intercalary cell and a duct cell) known as class 3 of Noirot and Quennedey (1991). The secretory cell has several large multivesicular electron‐lucent bodies, indicating a glycoprotein product associated with lipids. We hypothesize that this secretion protects the surface of antennae and sensilla from wear. The second group of glands includes unicellular glands known as oenocytes (class 2 of Noirot and Quennedey, 1991), which secrete epicuticular hydrocarbons through epidermal cells.     

Ultrastructural ontogeny of the labial gland apparatus in termite Prorhinotermes simplex (Isoptera, Rhinotermitidae)

The labial glands in Prorhinotermes simplex consist of secretory cells organized into acini, water sacs and the ducts connecting the gland parts to the basis of the labium. Acini are composed of central and parietal cells. Central cells type I contain predominantly lucent vacuoles and are involved probably in hydroquinone production. They are lacking in soldiers. Type II central cells produce vacuoles of proteinaceous content which are of the same electron density (type IIa) or present in more shades (type IIb). Type IIa cells are present in all older individuals, whereas type IIb are lacking in soldiers and neotenics. Type III cells represent a specific stage of type I cells development, but they are definite functional secretory cells in soldiers. Acini of first instar larvae contain undifferentiated cells which differentiate into type I cells during the second instar. Specific larval central cells start to change into type II cells during first instar. The central cells of presoldiers show a transition from the pseudergate into the soldier situation. The parietal cells keep a uniform structure throughout the whole ontogeny. Only one type of cells form the water sacs in all castes. The cells are very flat with scarce organelles. The water sac cells produce lipid-like secretion, small lucent vacuoles and bunches of angulated vacuoles. The water sac probably functions as water storage organ only. Ontogenetical changes in water sac development are small. The acinar ducts originate inside the acinus where they are formed by flat cells with rare organelles. At the acinus border, cells equipped with mitochondria, microvilli and basal invaginations appear. The water sac ducts are formed by flat cells with rare organelles. Acinar ducts outside the acinus and water sac ducts are equipped with taenidiuam.     

Ultrastructure of the principal and accessory submandibular glands of the common vampire bat

The principal and accessory submandibular glands of the common vampire bat, Desmodus rotundus, were examined by electron microscopy. The secretory endpieces of the principal gland consist of serous tubules capped at their blind ends by mucous acini. The substructure of the mucous droplets and of the serous granules varies according to the mode of specimen preparation. With ferrocyanide-reduced osmium postfixation, the mucous droplets are moderately dense and homogeneous; the serous granules often have a polygonal outline and their matrix shows clefts in which bundles of wavy filaments may be present. With conventional osmium postfixation, the mucous droplets have a finely fibrillogranular matrix; the serous granules are homogeneously dense. Mucous cells additionally contain many small, dense granules that may be small peroxisomes, as well as aggregates of 10-nm cytofilaments. Intercalated duct cells are relatively unspecialized. Striated ducts are characterized by highly folded basal membranes and vertically oriented mitochondria. Luminal surfaces of all of the secretory and duct cells have numerous microvilli, culminating in a brush borderlike affair in the striated ducts. The accessory gland has secretory endpieces consisting of mucous acini with small mucous demilunes. The acinar mucous droplets contain a large dense region; the lucent portion has punctate densities. Demilune mucous droplets lack a dense region and consist of a light matrix in which fine fibrillogranular material is suspended. A ring of junctional cells, identifiable by their complex secretory granules, separates the mucous acini from the intercalated ducts. The intercalated ducts lack specialized structure. Striated ducts resemble their counterparts in the principal gland. As in the principal gland, all luminal surfaces are covered by an array of microvilli. At least some of the features of the principal and accessory submandibular glands of the vampire bat may be structural adaptations to the exigencies posed by the exclusively sanguivorous diet of these animals and its attendant extremely high intake of sodium chloride.     

Fine structure and histochemistry of the epidermis of the fish Monopterus cuchia

An attempt is made to correlate fine structure with the histochemical reactions of the epidermis in the synbranchiform fish Monopterus cuchia. Three sources of mucus are identified. Superficial epithelial cells produce weakly acidic glycoprotein which is secreted at the surface as the external mucous layer or cuticle. Numerous large unicellular mucous glands have a secretion which is strongly acidic and sulphated, although the basal and peripheral parts of these cells, which contain most of the rough endoplasmic reticulum, react strongly for neutral glycoprotein; Golgi cisternae appear to be involved in a change of histochemical reaction from neutral to strongly acidic as the secretion is formed. A second, slender, type of mucous gland cell, not previously reported, gives a weaker reaction for sulphated acidic glycoprotein and has cytoplasm with numerous Golgi cisternae and free ribosomes, producing electron–dense secreted drops. Sacciform cells, with a protein–aceous secretion, have a characteristic fine structure with membranous "bubbles" at the surface of the cytoplasm. Ionocytes, sensor) cells and intrusive leucocytes have been identified in the epidermis.     

Fine structure of the axillary gland in the brown bullhead (Ictalurus nebulosus)

The axillary glands of Ictalurus are lobulated invaginations of the epidermis, opening at a pore between the pectoral spine and the cleithrum. Holocrine cells lining a false lumen form a viscous secretion. The secretory cells originate in the tenuous basal layer of the gland wall. Secretion is initiated by the formation of compound vesicles in cells that become very large and have complex cytoplasm of a varied appearance. Golgi systems are well developed and the perinuclear cytoplasm may contain many mitochondria and sacs of ribosomal endoplasmic reticulum; some tracts of cytoplasm are vesicular and contain free ribosomes. Some cells contain numerous large lysosomes, and some have extensive contents of fibrillar masses imperfectly separated by membranes, that recall the appearance of the mucous secretion of goblet cells. The secretory cells break down, releasing the degenerating organelles, including the nuclei, into the false lumen. Some structures are still recognizable in the secretion even after it has been expelled, but the main part of the formed secretion consists of the mucus-like masses. Various leucocytes are found in the gland walls and embedded in the secretion. The fine structure differentiates the holocrine cells of the axillary gland from the club cells of the epidermis, and from the venom glands associated with the fin spines of catfishes. The function of the axillary gland secretion remains unknown.     

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.     

Ultrastructural study of the mental body of Hydromantes genei (Amphibia: Plethodontidae)

The mental glands of Hydromantes genei are considered a specialized form of the urodele serous cutaneous glands. Use of a variety of techniques of maceration and digestion as well as transmission electron microscopy (TEM) and scanning electron microscopy (SEM) has shown the three-dimensional morphology of secretory and myoepithelial cells. Secretory cells are pyramidal and rest on an almost continuous layer of myoepithelial cells. The latter have a long ribbon-like body from which branch off transversal and longitudinal processes with swallow-tailed ends. Cytoplasmic processes of secretory cells, containing irregular dense vesicles, squeeze through clefts between myoepithelial cells and may reach, at some points, the basal lamina. The interstices between myoepithelium and secretory cells are extraordinarily rich in nerve endings with clear vesicles. The glandular outlets appear as elliptical stomata in the superficial layer of the epidermis and are lined by horny cells, which invaginate to circumscribe the excretory duct. The morphological results indicate that the myoepithelium of Plethodontidae mental glands differ in some respects from that of amphibian serous cutaneous glands. A double polarity for the secretory cells is also suggested. © 1993 Wiley-Liss, Inc.     

The digital pads of the tree frog, Hyla cinerea. II. The mucous glands

The mucous glands consist of a single row of cells surrounded by smooth muscle. The cells are attached at their apical and basal regions and only cytoplasmic projections loosely link the lateral aspects of adjacent cells. Material accumulates in the cisternae of the rough endoplasmic reticulum, appears to form into dense granules in the Golgi apparatus, and then before being secreted, undergoes chemical and morphological alterations. Since some glands secrete onto the dorsal epidermis of the digits, the mucous is believed to function as a wetting agent for the skin as well as an aid to climbing.     

光魟毒腺的显微和超微结构

为探讨魟类螫伤机理,用光镜和电镜观察了光魟的毒棘腹外侧纵沟内的毒腺的组织结构。结果表明：光魟的毒腺为复层上皮。从基底面到游离面依次为基底层、棘细胞层和嗜酸性细胞层。基底层细胞和棘层的细胞嗜碱性,棘细胞间有少量、散在分布的嗜酸性细胞;棘细胞的外层至腺上皮的游离面的嗜酸性细胞密集排列。电镜下可见基底细胞有丰富的核糖体。棘细胞内粗面内质网、高尔基复合体等较丰富。嗜酸性细胞内有电子密度低的膜包分泌颗粒;接近表面的细胞内颗粒部分融合;表层细胞核消失,胞质充满融合的颗粒,游离面侧的胞膜呈角质样增厚。腺上皮内还可见到黑色素细胞、郎格罕细胞和梅克尔细胞。提示毒腺组织内有两种类型的细胞,一类为毒液形成细胞,另一类为非毒液形成细胞。嗜酸性细胞内的电子密度低的膜包分泌颗粒成分可能是造成螫伤剧痛及全身症状的关键因素。     

Ultrastructure of male accessory glands of Chrysomya megacephala (Fabricius) (Diptera: Calliphoridae)

The ultrastructure of the male accessory glands of the blow fly, Chrysomya megacephala (Fabricius), was presented using light microscopy (LM), scanning electron microscopy (SEM), and transmission electron microscopy (TEM). A pair of accessory glands was separated at opposite sites. Morphometric results using LM yield evidenced no significant difference in the median of either length or width of the left and right glands. A significant increment in both length and width was seen to plateau between three to six days. SEM observation showed that the surface of the glands revealed a faint irregular groove pattern throughout, and it was occasionally penetrated by tracheoles. Each gland was a slender, elongated sac‐like tubule having apical rounded ends, with a slight constriction at the sub‐apical part of the gland being observed occasionally. TEM analyses of three‐day‐old males showed that the glands consisted of external capsular cells with a basement membrane underneath, glandular cells, and gland lumen. The capsular cell was flat and contained a nucleus with electron dense material in the nuclear envelope. The glandular cell, appearing as columnar, consisted of a vacuolated component that contained a large oval nucleus centrally or sub‐basally located, with dense mitochondria, numerous rough endoplasmic reticulum, and secretory vesicles containing electron‐lucent materials. In the gland lumen, the cross‐section through the middle portion revealed dense secretory materials, characterized by electron‐dense materials. Some sections revealed a large lumen where secretion accumulates within the delicate sac. The seven‐day‐old glands exhibited a remarkable change in the lumen, where the whole space contained a large amount of secretory materials, with the electron‐dense materials being characterized as similar to those observed in three‐day‐old glands. About four prominent types of secretions were observed on the basis of difference in electron‐density.     

Electron microscopic studies on the pars intermedia in normal and in mice with hereditary nephrogenic diabetes insipidus

Summary The ultrastructure of the pars intermedia (PI) of the normal VII +/+ and hereditary nephrogenic diabetes inspidus DI Os/+ mice has been studied with particular reference to the morphology of the glandular cells and their innervation. Four types of cells were observed in both the genotypes of mice, 1) the light glandular cell, 2) the dark cell, 3) a type of cell similar to ependymal cells and 4) a small percentage of typical ACTH cells, observed mostly on the PI border of the cleft and rarely in the centre of PI. The predominant light glandular cells contain mainly two types of membrane bound granules: 1) electron dense core granules, which measure 1500–2500 Å and 2) electron lucent vesicles, which measure 3000–4000 Å in diameter. Granules of intermediate size with various density are also present in both types of mice. The electron dense core granules are predominant in DI Os/+ mice, whereas, electron lucent vesicles are predominant in the normal VII +/+ mice. Similar uniform size membrane bound electron dense granules have been observed in ACTH cells of PI and pars distalis. From earlier experimental evidences and the present observations, it is concluded that the dense core granules in PI may be synthesizing ACTH or ACTH-like substance. It is also discussed that these dense core granules may further mature and give rise to MSH in the form of electron lucent vesicles. If it is so, PI light glandular cells may have dual functions, of producing MSH and ACTH. One of the functions of ependymal-like cells, may be the transport of PI secretion.Three types of nerve endings are observed throughout the PI, making synaptic contact with the predominant cell type. The innervation is more in DI Os/+ mice than in normal mice. The classification of these nerves is according to Bargmann and co-workers 1) peptidergic neurosecretory fibers, contain mainly membrane bound dense core granules, measuring 1200 to 1800 Å, and are the classic neurosecretory granules; 2) adrenergic fibers, measuring 700–900 Å; 3) cholinergic fibers, measuring 300–400 Å. Adrenergic and cholinergic fibers are more towards the hypophysial cleft. The increased innervation, the synaptic contact, the extremely hypertrophied PI and the greater activity of its light glandular cells in the DI Os/+ mice show the PI is under the influence of the nervous system.This study was supported by MRC of Canada Grant No. MA-3759.     

Seasonal ultrastructural variations in pinealocytes of the woodchuck,Marmota monax

The ultrastructure of the pinealocyte in the woodchuck, Marmota monax, was studied during the four seasons of the year. Fall cells have a fairly uniform cytoplasmic density, organelles consistent with synthetic and/or secretory activity and rather extensive pericapillary and intercellular spaces. Many winter pinealocytes are nearly devoid of ribosomes and granular endoplasmic reticulum but contain lipid droplets associated with mitochondria. Pericapillary and intercellular spaces are minimal. Spring glands have the greatest variation in cytoplasmic density with intercellular and pericapillary spaces similar to that seen in fall glands. Cells containing electron dense cytoplasm have Golgi zone associated, secretory granules, free ribosomes, short sections of granular endoplasmic reticulum and dense bodies. Cells with a more electron lucent cytoplasm are similar to the most frequently observed summer pinealocytes which have numerous Golgi zones but few associated secretory granules. Microtubules are prominent in the cytoplasm of these cells, the plasma membranes are smooth and intercellular and pericapillary spaces are minimal. A yearly rhythm or cyclic activity of the pinealocyte is suggested.     

Ultrastructure of the rotifer integument: peculiarities of Sinantherina socialis (Monogononta: Gnesiotrocha)

The rotifer integument is a well‐described syncytium that contains an apical intracytoplasmic lamina (ICL) that functions for both skeletal support and muscle insertion. To date, there is limited information on the structure of the integument in species of Gnesiotrocha, a diverse subclade of Monogononta that consists of solitary, colonial, sessile, and planktonic species. In this study, we examined the ultrastructure of the integument in the colonial rotifer Sinantherina socialis to determine how it corresponds to that of other monogononts. The integument of S. socialis was broadly similar to that of other rotifers, consisting of a thickened glycocalyx, multilaminate ICL, and syncytial epidermis. However, it was different in several regards. The ICL consisted of three distinct layers from apical to basal: layer 1 consisted of at least two electron‐dense laminae; layer 2 was a thickened matrix of amorphous, electron‐dense material or was fibrous; and layer 3 was an electron‐dense lamina of varying thickness that covered the underlying syncytium. Significantly, layers 1 and 2 formed a ridge‐and‐groove like system of finger‐like projections across the trunk surface that has not been observed in other rotifers. A voluminous syncytial cytoplasm (up to 3 μm thick) was present beneath the ICL and was mostly electron lucent and with few organelles. Bundles of potential microtubules were scattered throughout the syncytium. We hypothesize that the voluminous cytoplasm with microtubules serves as skeletal support for the rotifer's sessile lifestyle, while the external ridges may function as a texture‐based deterrent to predators, or serves to trap secretions from the species' defensive glands. Basally, the epidermis was highly folded and bordered by a thin basal lamina that separated the plasmalemma from the blastocoel. Membrane‐bound vesicles were present throughout the integument's cytoplasm and are hypothesized to function in the secretion of extracellular matrix and in the maintenance of the ICL.     

Tail skin of the dipnoan Neoceratodus larva: fine structure and differentiation

The fine structure of the tail skin oflarval Neoceratodusforsteri , between stages 40 and 50 (Kemp, 1982), is described and where applicable specific cellular components are compared and contrasted with comparable ones in the skin of adult dipnoans, teleosts and larval and adult amphibians.
The epidermis of the early developing tail, within the range studied, differentiates a variety of different cell types. Surface epithelial lucent and vacuolated lucent cells and basal cells are distinguished, and goblet (mucous) cells, Merkel cells and macrophages appear in the epidermis towards the end of the series.
Below a poorly developed collagenous basement lamella, immature melanophores with premelanosomes are present, and likewise there are non–myelinated nerves, some striated muscle fibres, capillaries and mesenchymal fibroblasts.
The tail epidermis is innervated by naked neurites from the beginning of the series, and the earliest recognizable Merkel cell is in synaptic association with neurites.