Extensive Endoplasmic Reticulum Research Articles

Ultrastructure of the Genital Duct Epithelium of the Male Port Jackson Shark, Heterodontus-Portusjacksoni

The genital ducts of Heterodontus portusjacksoni are lined by a ciliated epithelium. In the ductuli efferentes the epithelium is low and contains numerous intraepithelial leucocytes which often contain large dense bodies. All epithelial cells are ciliated and are characterised by apical vesicles, vacuoles and glycogen granules, some rough endoplasmic reticulum, dense bodies and lipid droplets, and a Golgi apparatus. The initial segment of the ductus epididymidis is lined by a very tall epithelium of ciliated and non-ciliated cells. The non-ciliated cells contain numerous apical vesicles, a large Golgi apparatus and numerous mitochondria and secretory granules in close association with an extensive endoplasmic reticulum. The terminal segment of the ductus epididymidis is lined by a low columnar epithelium. A proximal region, occupying part of the head of the epididymis, is similar to the epithelium in the ductuli efferentes. Distally, all the epithelial cells are ciliated. They are characterised by considerable dilated endoplasmic reticulum, a Golgi apparatus, apical vesicles, and numerous mitochondria and secretory granules. The secretory tubules of Leydig's glands are lined by a very tall epithelium with non-ciliated cells containing extensive, dilated, rough endoplasmic reticulum, a large Golgi apparatus, and numerous mitochondria and secretory granules. The significance of the structural differentiation of the duct is discussed in relation to the evolution of the mammalian epididymis.

Comparative ultrastructure of lipid storage sites in femaleEuchaeta marina andPleuromamma xiphias (Copepoda: Calanoida)

FemaleEuchaeta marina (Prestandrea, 1833) have one large, thin-walled lipid sac, whereas femalePleuromamma xiphias (Giesbrecht, 1889) have two separate and morphologically distinct lipid storage sites. One lipid site inP. xiphias corresponds to the mesenteric tissue that surrounds the anterior region of the midgut. The morphology of these cells resembles that of mammalian brown adipocytes. The cytoplasm is filled with extensive smooth endoplasmic reticulum, numerous mitochondria and several deposits of intracellular lipid. The second lipid site ofP. xiphias lies in the posterior region of the metasome and resembles the thin-walled lipid sac ofE. marina. Both lie adjacent to, but are not contiguous with, the narrow mesenteric tissue surrounding the last region of the midgut. Both sacs contain a single, large deposit of intracellular lipid enclosed by a very thin rim of cytoplasm and resemble mammalian white adipocytes. The different habitats and reproductive processes of these two copepod species may relate to the observed variations in lipid cell morphology. The reserve lipid inE. marina plays a primary role in reproduction and is linked closely with the continuous cycle of oocytic maturation. The lipids synthesized and stored byP. xiphias, a strong vertical migrator, may be influenced by food availability, a function of their mesopelagic habitat. The primary role of the reserve lipids in this copepod may be to provide energy during migrations and between feeding periods, with relatively less lipid being allocated to reproduction.

The Structure and Cytochemistry of the Pistil of Sternbergia lutea (Amaryllidaceae)

Studies were carried out on structural and cytochemical aspects of the pistil of Sternbergia lutea (L.) KerGawl. The stigma is of the wet papillate type; the papillae are unicellular and are arranged densely around the rim of a funnel-shaped stigma. The stigma exudate is limited and is confined to the bases of the papillae and the inner lining of the stigma. The papillae are smooth in the distal part and are covered with intact cuticle-pellicle lining. The cuticle is disrupted at places towards the base of the papillae releasing the exudate. The exudate is rich in pectins and other polysaccharides but poor in proteins and lipids. The papillae show dense cytoplasmic profiles with extensive endoplasmic reticulum (ER), abundant mitochondria, polyribosomes and active dictyosomes. The style is hollow. The stylar cavity is surrounded by two to four layers of glandular cells. In the young pistil the canal is lined with a continuous cuticle, but in the mature pistil the cuticle becomes disrupted and the canal is filled with the secretion produced by the cells of the surrounding glandular tissue. Ultrastructurally, the cells of the glandular tissue are very similar to the stigmatic papillae. The inner tangential wall of the cells bordering the canal is uniformly thicker than other walls. The secretion in the stylar canal, as well as the intercellular spaces of the glandular tissue, stain intensely for pectins and polysaccharides but poorly for proteins and lipids. Pollen tubes grow through the stylar canal. Structural and cytochemical details of the pistil of Sternbergia are compared with other hollow-styled systems.

Ultrastructure of substance P immunoreactive elements in the periaqueductal gray matter of the rat

Substance P (SP) is a non-opioid peptide that generates a potent analgesia when injected into the periaqueductal gray matter (PAG). The aim of this study was to investigate the fine neuronal structures and synaptic circuits involved in SP action in rats by means of electron microscopy, using immunocytochemical (ICC) pre-embedding methods. A conventional ultrastructural study, carried out to interpret the ICC data correctly, shows small sized nerve cell bodies with a high nucleus-cytoplasmic ratio; absence of an extensive granular endoplasmic reticulum; and few axo-somatic contacts having symmetrical and asymmetrical junctions in equal proportions. The large neuropil is characterized by numerous thin unmyelinated axons and axo-dendritic synapses mainly showing pleomorphic vesicles and asymmetrical junctions. The ICC analysis showed moderately labeled nerve cell bodies with the same structural, synaptic, and dimensional features as the negative cells. In the neuropil SP immunoreactivity is shown by dendrites, synapses, and thin elements which are unidentifiable structurally. No SP terminals synapsing on SP nerve cell bodies were found and only occasional SP light labeled terminals synapsing on negative perikarya were seen. The SP boutons generally have pleomorphic vesicles and asymmetrical junctions. On the basis of these data a possible excitatory activity of PAG SP synapses could be hypothesized. This activity would take place on postsynaptic neurons generally at a dendritic level. Our ultrastructural findings give support to an excitatory role carried out by SP neurons of the PAG, as suggested by the role of PAG circuitry on spinal nociception.

Pollen tube tip growth.

This review considers pollen tube growth with regard to current information on pollen tube cytoplasm, wall structure and calcium ion interactions with pollen tubes. Pollen tubes have a marked cytoplasmic Polarity with a number of distinct zones along the tube, each with a characteristic complement of cytoplasmic and nuclear structures. The cytoplasmic structures are characteristic of secretory cells with extensive endoplasmic reticulum cisternae and numerous dictyosomes. The dictyosomes produce secretory vesicles that are mainly directed to the extending tip of the tube, where they provide new plasma membrane and wall components. The rates of secretory vesicle production and delivery have been estimated, allowing quantitative assessments of the rate of delivery of materials to the tip. Pollen tubes contain cytoskeletal components, with microtubules and microfilament strands lying axially in the main tube and diffuse microfilament strands at the tip. The tube wall consists of an outer fibrous layer containing pectins and an inner, more homogeneous layer containing callose and cellulose-like microfibrils, possessing both β-1,4 and β-1,3 linkages. Protein is also present in the wall. The tube tip lacks the inner callosic wall. This type of structure is considered to be different from that of elongating sporophyte tissue cells which are enclosed by a wall containing layers of cellulose microfibrils. Calcium ions are required for pollen tube growth and, in at least some species, act as a chemotropic agent. High concentrations of calcium ions in the external medium inhibit growth. Pollen tubes contain some calcium ions bound to the cell wall and larger amounts located intracellularly, which enter the tube at the tip. This intracellular calcium is present as ions that exist freely within the cytoplasmic Matrix and as ions bound to membrane systems. The highest concentrations in both of these pools are found at the tip and in both they decline towards the base. The structure of the tip and the activity involved in providing components for plasma membrane and Wall assembly provide a basis for considering possible mechanisms of tip growth. Two hypotheses to account for the regulation of tip extension are considered, cell wall control and cytoskeletal control. In the cell wall hypothesis, control depends on an interaction between internal turgor pressure and a plastic cell wall. The mechanical properties of the wall are assumed to be partly dependent on the availability of external calcium ions to crosslink acidic pectin chains. According to this hypothesis, high external calcium ion concentrations cause cessation of tip growth due to increased mechanical resistance of the tip wall. Various observations on plant cell-wall interactions with calcium ions and on experimentally-treated pollen tubes provide evidence that does not support this hypothesis. The cytoskeletal control hypothesis of tip growth depends on the internal tip cytoskeleton to contain the tube tip cytoplasm against the internal turgor pressure during cell wall assembly. The activities and mechanical properties of the cytoskeleton are assumed to depend on the availability of external calcium ions. High external concentrations are believed to cause a state of rigor in the cytoskeleton and hence a cessation of tip growth. Some experimental evidence is presented which suggests that the effects of excess calcium ions are on intracellular processes, and not extracellular ones. The mitochondrial zone behind the tip is believed to maintain the tip calcium ion concentration at an optimal level for growth. Some comparisons are made between tip growth in pollen tubes and that in other tip growing cells. CONTENTS Summary 323 I. Introduction 324 II. Cytoplasm 326 III. Wall structure 332 IV. Calcium 335 V. Tip growth 339 VI. Conclusions 350 References 351.

CULTURING, ULTRASTRUCTURE AND COLONY FORMATION INPECTODICTYON CUBICUM(CHLOROPHYCEAE, CHLOROCOCCALES)12

ABSTRACTPectodictyon cubicumTaft collected in California develops typical eight‐celled, cuboidal colonies only in alkaline media. Vegetative cell ultrastructure is similar to that in other genera of the Chlorococcales, except for an extensive endoplasmic reticulum system paralleling the plasmalemma (termed a paramural ER). Autosporogenesis proceeds inside the parent cell wall by three mitotic divisions producing eight nuclei in two tiers of four. Cleavage furrows following paths delineated by long ER segments and indistinct microtubules bisect and then radically separate the protoplast into eight pyramidal units. Walls comprised of a thick, presumably cellulose layer and a thinner trilaminar layer (not acetolysis resistant) form as cells become rounded, except where touching. A gelatinous matrix is produced around and between cells with concentration at the three sites of prior cell contact 90 degrees apart. Pulsed production of mucilage in three solid strands forces cells to separate, and the expanding colony becomes a hollow cube with a cell at each corner.

Cytogenetic evidence that the malignant event in multiple myeloma occurs in a precursor lymphocyte

Multiple myeloma is traditionally thought of as a disease of plasma cells. Evidence from studies using antiidiotype antibodies, however, suggests that malignant events may take place in a precursor lymphocyte perhaps as early as the pre-B cell. In this study, we present cytogenetic evidence to support the latter view. Peripheral blood was obtained from a patient with plasma cell leukemia and light chain disease. Karyotypic analysis, using Giemsa banding techniques, showed an abnormal karyotype: 44,XY,−6,−8,−13,−16,−22, +mar1,+mar2,+mar3,del(1)(p22,p32),11p+,13q+,14q+. A suspension culture was established and a plasma cell line was grown. It was characterized by transmission electron microscopy as having an eccentric nucleus, abundant cytoplasm, and extensive endoplasmic reticulum. A subculture of this line was subsequently grown that was characterized by transmission electron microscopy as a lymphoid cell with diminished quantity of cytoplasm without extensive endoplasmic reticulum. Karyotypic analysis of the smaller cell demonstrated a modal number of 88 chromosomes and was a tetraploid derivative of the first. Our study provides cytogenetic evidence that cells with a lymphocytic phenotype show karyotypic abnormalities seen in the malignant plasma cell of the same patient, and thus, can be considered as evidence favoring the initiating cell of plasma cell myeloma as being an early B lymphocyte.

Light and electron microscopy of the new born sagittal suture.

Morphogenesis and maturation of the sagittal suture in newborn C57B1/6J strain mice were studied using light and electron microscopy. Morphodifferentiation of the murine parietal bones progresses radially with the interposed sagittal suture, assuming a greater level of maturity at birth at a midpoint along its length. The presumptive suture develops in a sulcus, deeper posteriorly, more shallow anteriorly. Cells at the osteogenic front (OF) are distinguished from the surrounding fibrocytic cells by a number of distinctive characteristics: 1. increased cytoplasmic density; 2. extensive endoplasmic reticulum; 3. dispersed nuclear chromatin aggregates; 4. extensive surface projections; 5. close approximation. Mineralization of the developing parietal bone occurs extracellularly with the initial deposits of apatite crystals exhibiting no oriented relationship to either cellular or extracellular fibrillar elements. The majority of collagen fibers lie superior and inferior to the presumptive suture, oriented anteroposteriorly with their long axes parallel to the ectocranial surface. Other fiber bundles more intimately associated with the developing suture display a more random orientation.

Retinoids alter the direction of differentiation in primary cultures of cutaneous keratinocytes

The effects of vitamin A on the morphological expression of differentiation were studied in cell cultures of cutaneous keratinocytes from the newborn rat. The cells were first cultivated in a medium containing 0.11 m M calcium until a confluent monolayer had been formed. Stratification and terminal differentiation were then triggered by raising the calcium concentration of the medium to 1.96 m M (‘normal’ culture). The rise in the concentration of calcium was coupled with the addition of retinol (RL) or retinoic acid (RAC) to the medium to produce an excess of vitamin A (high-retinoid culture). Delipidized serum was used to produce a deficiency of vitamin A (low-retinoid culture). The tissue organization and the ultrastructure of the keratinocytes in the stratified culture were the same as those seen in conventional cultures and skin explants. These stratified cultures expressed the morphological features of the epidermis of intact skin. The addition of RL or RAC to the medium enhanced features characteristic of the secretory epithelium, such as the formation of an extensive endoplasmic reticulum, an enlargement of the Golgi zone, and an increase in the number of vacuoles. At the same time, the addition of retinoids diminished features characteristic of the terminal differentiation of the stratified squamous epithelium, such as stratification and keratinization. Deficiency of vitamin A in the medium resulted in a culture with many differentiated layers. The differentiated cells of the low-retinoid cultures contained densely packed tonofilaments and synthesized products that reacted with the monoclonal antibody AE2 that is specific for keratin peptides which are markers of epidermal differentiation. In the cell culture system that is presented here, an excess of retinoids redirected epithelial differentiation from a stratifying and keratinizing epithelium towards a secretory epithelium. This system is a useful tool for elucidating the mechanisms responsible for the effect of vitamin A on the differentiation of epithelial cells.

Effects of zinc on epidermal ultrastructure in the larva of Clupea harengus

In March, 1983 changes in epidermal ultrastructure were examined in Clupea harengus L. larvae hatched from eggs incubated in four zinc concentrations (0.5 2.0, 6.0 and 12.0 ppm). In addition to the outer and inner epidermal cell types described previously, a third type of cell is present. Ultrastructurally this resembles the epidermal “chloride cells” of Sardinops caerulea Girard, characterised by numerous mitochondria, extensive smooth endoplasmic reticulum and a free surface exposed to the environment. These cells occur on the yolk sac, head and in the regions of the trunk just above the yolk sac. In larvae treated in 12.0 ppm zinc, the cells contain fewer mitochondria with fewer cristae than those in the controls. Smooth endoplasmic reticulum is much reduced forming nodular masses and contains granular osmiophilic inclusions. In larvae hatching from eggs previously incubated in 6.0 and 12.0 ppm zinc, the epidermal cells contain more vesicles, intracellular spaces, and swollen mitochondria and show signs of necrosis. The viability of these larvae is discussed.

Morphology of salp chain communication

The plaque consists on one side of a small button of modified epithelial cells (plate 1, 5 and 6) and on the other of a small group of sensory cells, which are less conspicuous than the button cells. At the light microscope level, the button cells can be seen to form a sort of small button or mushroom protuding from the epithelium of the plaque (plate 1, 11 and 12; figure 2) into the test material separating the two epithelial layers. Opposite this button are a group of sensory cells, the axons of which pass to the brain shrouded in the bases of the epithelial cells (plate 1, 8 and 9). The arrangement of the button cells and opposing sensory cells is a constant one, so that, on a single zooid, one of the pair of plaques joining it to an adjacent zooid has a group of sensory cells, the other (the non-innervated plaque), a group of button cells. The plaques at the outer ends of the horns are innervated, as are those near the horn bases, while those on the ventral surface and at the inner end of the horns are not innervated, and have the button cells. In consequence of this, it is a simple matter to separate one or other of the plaques joining two zooids to investigate their physiological properties (Anderson & Bone 1980). Fedele (1920) first described the sensory cells of the attachment plaques, but he supposed that they occurred at both sides in each plaque. In fact, they lie only on one side of the plaque, as described above, and this asymmetry has important consequences for the way in which the system operates. Apart from the specialized region of the plaque, where these cells are found, the plaque is symmetrical, and the two epithelial layers are some 5 μm apart, separated by test material (plate 1, 7). The epithelial cells are flattened (like those of the outer epithelium outside the plaques), and are some 2–5 pm thick (plate 2, 1). They contain an extensive smooth endoplasmic reticulum, mitochondria with tubular cristae, flattened nuclei, and occasional vesicles of various sizes

PCC4azal teratocarcinoma stem cell differentiation in culture: II. Morphological characterization

The ultrastructural morphology of the PCC4azal embryonal carcinoma cells and their differentiated counterparts, endoderm-like cells and giant cells, was characterized and compared with that of the cells of embryoid bodies. The ultrastructure of the PCC4azal embryonal carcinoma cells is similar to that of the embryonal carcinoma cells of the embryoid body. These cells are small, with a large nucleus and relatively few cytoplasmic organelles. Gap junctions and modified adherens junctions are formed at some areas of intercellular contact between the embryonal carcinoma cells. The differentiated PCC4azal endoderm-like cells have a more developed cytoplasm, containing an extensive endoplasmic reticulum with large Golgi regions. Most striking is the de novo appearance of epithelial-like junctional complexes which join the apical borders between the endoderm-like cells, thus polarizing the cell monolayer. The zonula occludens junctions of the junctional complex are extensive, consisting of six or more strands of tight junctional ridges. Terminal webs are present in the apical regions that are inserted into the zonula adherens region of the junctional complex. Gap junctions continue to join neighboring cells, and some gap junctions are intercalated within tight junctional ridges. The ultrastructure of the differentiated endodermal cells of the embryoid bodies is very similar to that of the PCC4azal endoderm-like cells. The embryoid body endodermal cells form similar junctional complexes which also contain continuous belts of tight junctions that are intercalated with gap junctions. As the PCC4azal endoderm-like cells are transformed to giant cells, a massive cytoskeleton is formed, consisting of a large complex system of 10-nm filaments, microtubules, and 7-nm microfilaments. The junctional complexes that were present during the endodermal stage are partially disassembled as the giant cells migrate apart. Thus, the differentiation process in this system is characterized by significant and distinctive morphological changes.

An electron microscopic study of lipid absorption in the pyloric caeca of rainbow trout (Salmo gairdnerii) fed wax ester ? rich zooplankton

Rainbow trout were killed 4 and 18 h after being fed wax ester-rich marine zooplankton and the absorptive epithelium of the pyloric caeca examined by electron microscopy. Numerous osmiophilic drops were seen in the lamina propria underlying the epithelium of fish killed at both times, but these drops were only abundant within columnar epithelial cells of fish killed 4 h after feeding. Pinocytotic profiles were not common at the luminal plasma membranes, nor were osmiophilic droplets seen in the terminal web area between the luminal plasma membrane and the extensive smooth endoplasmic reticulum. Numerous osmiophilic droplets, 30--100 nm in diameter, were present in the cisternae of the smooth endoplasmic reticulum with up to five separate droplets per individual cisterna. Columnar epithelial cells also contained up to 100 large osmiophilic drops ("conglomerates") which tended to be concentrated in the supranuclear (Golgi) regions. The conglomerates were 250--1200 nm in diameter and were themselves made up of smaller droplets 30--400 nm in diameter. Conglomerates were present both within intracellular membranes and free in the cytoplasm. Osmiophilic droplets in the intercellular spaces and lamina propria were similar in size to individual droplets within conglomerates. We conclude that triacylglycerols are elaborated in the smooth endoplasmic reticulum, transferred to and processed in the Golgi region and finally discharged serosally as chylomicron-like particles of not greater than 400 nm diameter.

Evidence for the zonation of interrenal tissue in the adrenal gland of the duck (Anas platyrhynchos).

Although interrenal tissue from the intact duck does not show a clear zonation when examined by light microscopy, the tissue does develop a well defined zonation following exposure to high and low levels of corticotropic stimulation. Under these conditions clear ultrastructural differences are seen between cells of the subcapsular zone (SCZ) and the inner zone (IZ). Based on these observations, the ultrastructure of tissue from intact birds was examined retrospectively and in addition, cell sizes and the relative volumes and areas of intracellular components were measured morphometrically. These analyses reveal morphological and quantitative differences between cells from the IZ and the SCZ. Cells of the IZ have small rounded nuclei, extensive smooth endoplasmic reticulum (SER) and mitochondria with tubular cristae, whereas cells from the SCZ contain pleomorphic nuclei, less SER and mitochondria with shelf-like cristae. The mean cell volume in the IZ is significantly less than that in the SCZ. In the SCZ cells the volume densities (volume per unit volume cytoplasm) of mitochondria and lipid droplets and the surface densities (area per unit volume cytoplasm) of the outer mitochondrial membranes are significantly greater than those in IZ cells. Conversely, in the cells of the IZ the volume densities of the nuclei and dense bodies and the surface density of the SER are greater than the corresponding values estimated for the cells of the SCZ. Although the mitochondria comprise a smaller fraction of the mean volume of IZ cells than SCZ cells, the total surface area of the cristae is approximately the same in the cells of both zones.

Ultrastructure of the respiratory epithelium in the lungs of the tortoise, Testudo graeca

The respiratory epithelium in the lungs of the tortoise (Testudo graeca) has been studied by electron microscopy. The epithelium consists of a mosaic of two different cell types (here called "pneumonocytes"). Type I pneumonocytes are roughly squamous and possess attenuated flanges of cytoplasm which extend over the septal capillaries. Localized cytoplasmic expansions are often present near the periphery of these flanges. Most of the organelles are concentrated in the perinuclear region; the most prominent of these are the mitochondria and osmiophilic inclusions. In contrast, type II pneumonocytes are cuboidal and are richly endowed with organelles including large Golgi complexes, extensive endoplasmic reticulum and numerous inclusion bodies. The morphological evidence suggests that type I pneumonocytes are involved in the secretion of osmiophilic material (presumed to be pulmonary surfactant) and in maintaining the integrity of the air-blood barrier. Type II pneumonocytes appear to be concerned solely with the production of surfactant.

Ultrastructure of Oil Gland Development in the Leaf of Citrus sinensis L.

The young oil glands of Citrus sinensis L. consist of a central group of polyhedral cells encircled by layers of radially flattened cells The oil chamber forms schizogenously through a separation of the walls of the central cells, which are pushed outward and flattened with the expansion and filling of the oil chamber. With further expansion of the chamber, the surrounding cells become vacuolate and fragile, and there are indications of wall degradation suggestive of lysigeny of the cells at this stage. The extensive endoplasmic reticulum in the central cells of the young glands is suggested as the primary site of synthesis of the essential oil.

Electron Microscopic Observations on Rat Epidermis During Experimental Carcinogenesis

Early ultrastructural changes and their progressive evolution were studied in rat epidermis following topical application of carcinogen (3-methylcholanthrene) and were compared to ultrastructural features of fully developed tumors (sebaceous epithelioma and basal cell epithelioma) in animals of the same group. Similar cytologic alterations were found, such as a marked increase in free ribosomes and polysomes, extensive endoplasmic reticulum, considerable increase of mitochondria, and dilated intercellular spaces, occupied by cytoplasmic projections. Predominance of dark cells, considered by us to be only phenotypically different from normal (light) cells, was also observed. A two-stage or multiple-stage of neoplastic evolution was suggested.

The Fine Structure of Oogenesis in Marchantia polymorpha

Archegonium development, beginning with the archegonial initial and culminating in the mature egg, was studied with the electron microscope. The ultrastructural features of the beginning stages in development of the archegonium are relatively similar to one another. Plasmodesmata occur between all adjacent cells at this time. After the secondary central cell is formed these protoplasmic connections are lost, and both axial and parietal cell lineages begin to show signs of ultrastructural differentiation. The mature egg is characterized by cytoplasm rich in ribosomes and larger organelles. Mitochondria and simplified plastids commonly display a juxtaposed association. As far as could be ascertained the numerous plastids and mitochondria in the egg of Marchantia arise through division of preexisting organelles and are not formed anew from evaginations of the nucleus. Blebbing of the nucleus produces polymorphic organelles which appear to be pinched off into the cytoplasm. The mature egg also contains vacuoles and lipid bodies toward its periphery, while dictyosomes and extensive endoplasmic reticulum occur throughout. The space between the wall cells and the mature egg appears to contain an amorphous substance. No extra membrane was observed around the mature egg.

THE FINE STRUCTURE OF OOGENESIS IN MARCHANTIA POLYMORPHA

Archegonium development, beginning with the archegonial initial and culminating in the mature egg, was studied with the electron microscope. The ultrastructural features of the beginning stages in development of the archegonium are relatively similar to one another. Plasmodesmata occur between all adjacent cells at this time. After the secondary central cell is formed these protoplasmic connections are lost, and both axial and parietal cell lineages begin to show signs of ultrastructural differentiation. The mature egg is characterized by cytoplasm rich in ribosomes and larger organelles. Mitochondria and simplified plastids commonly display a juxtaposed association. As far as could be ascertained the numerous plastids and mitochondria in the egg of Marchantia arise through division of preexisting organelles and are not formed anew from evaginations of the nucleus. Blebbing of the nucleus produces polymorphic organelles which appear to be pinched off into the cytoplasm. The mature egg also contains vacuoles and lipid bodies toward its periphery, while dictyosomes and extensive endoplasmic reticulum occur throughout. The space between the wall cells and the mature egg appears to contain an amorphous substance. No extra membrane was observed around the mature egg.

Effects of Menazon and Usnic Acid on Histochemical and Ultrastructural Changes During Germination of Mung Beans1

Abstract Menazon (S-(4,6 diamino-s-triazin-2-methyl) o,o-dimethyl phosphorodithioate) an organophosphate insecticide, and usnic acid, an allergen present in lichens, inhibited germination of mung bean (Phaseolus mungo L.). On the third day of germination, cotyledons were examined histochemically and ultrastructurally and the resultant photomicrographs showed abundant starch grains and protein bodies in the treated seeds compared to the controls. Electron microscopic examination showed extensive endoplasmic reticulum and ribosomes along with vacuoles and normal mitochondria in control tissue. In contrast, the presence of protein bodies and disruption of the cytoplasmic organization were conspicuous in the menazon- and usnic acid-treated mung beans. This suggests impaired utilization of food reserves during germination.