Desiccation causes the proliferation of multicellular hairs, but not mucilage papillae, in Cryptothallus mirabilis (Hepatophyta): a correlated light and electron microscope study

1990 ◽  
Vol 68 (3) ◽  
pp. 697-706 ◽  
Author(s):  
Jeffrey G. Duckett ◽  
Karen S. Renzaglia ◽  
Keith Pell
Keyword(s):  
Endoplasmic Reticulum ◽  
Electron Microscope ◽  
Acid Phosphatase ◽  
Endophytic Fungus ◽  
Electron Microscope Study ◽  
Secretory Phase ◽  
Golgi Bodies ◽  
Dense Cytoplasm ◽  
Thin Walled ◽  
Multicellular Hair

When Cryptothallus dries out over periods of 4–20 days, the dorsal surfaces of the thalli become covered with multicellular hairs. The distribution of mucilage papillae and the endophytic fungus are not affected by desiccation. The hairs are thin walled and highly vacuolated whereas the mucilage papillae, like their secretory counterparts in Marchantia and mosses, are thick walled with dense cytoplasm containing stacks of endoplasmic reticulum and numerous Golgi bodies. Cytochemistry shows that the secretion is rich in carbohydrates and is derived from Golgi vesicles. After an active secretory phase, senescence of the mucilage papillae is associated with acid phosphatase activity. Key words: Aneura, Cryptothallus, desiccation, liverwort, mucilage papilla, multicellular hair, ultrastructure.

The Effects of Calcium on the Ultrastructure of Cox's Orange Apples With Reference to Bitter Pit Disorder

1975 ◽  
Vol 23 (1) ◽  
pp. 55 ◽  
Author(s):  
HK Mahanty ◽  
BA Fineran
Keyword(s):  
Endoplasmic Reticulum ◽  
Electron Microscope ◽  
Microscope Study ◽  
Electron Microscope Study ◽  
Thin Sections ◽  
Golgi Bodies ◽  
Cool Storage ◽  
Bitter Pit ◽  
Intermediate Results

An electron microscope study on thin sections of epidermal, hypodermal and cortical tissues has been made of calcium-sprayed and unsprayed apples in relation to bitter pit disorder. Golgi bodies, endoplasmic reticulum, mitochondria, chromoplasts, vacuoles and groundplasm were better preserved in sprayed apples during cool storage for up to 2 months than in unsprayed samples. In unsprayed apples these organelles were often drastically changed. The nucleus remained reasonably well preserved in all samples. Apples from trees sprayed only once gave somewhat intermediate results.

Electron microscope study of the microgranules in human vaginal epithelium

1978 ◽  
Vol 36 (2) ◽  
pp. 568-569
Author(s):  
A. Campos ◽  
J. Vilches ◽  
J. Gomez
Keyword(s):  
Electron Microscope ◽  
Microscope Study ◽  
Intercellular Space ◽  
Electron Microscope Study ◽  
Vaginal Epithelium ◽  
Vaginal Mucosa ◽  
Secretory Phase ◽  
Cervical Epithelium ◽  
Keratinized Epithelium ◽  
Fertile Women

Microgranules have been described with different names in keratinized and in nonkeratinized epithelium. In keratinized epithelium it seems clear that the microgranules are lamellated bodies bounded by a membrane which empty their contents into the intercellular space. Their existence in nonkeratinized epithelium is more debatable. Until now the so-called microgranules have been described in nonkeratinized bucal, lingual and cervical epithelium. In the present work we describe the morphology and nature of such structures in human vaginal epithelium.Biopsies from the midlevel of the vaginal mucosa were taken from voluntary fertile women. The specimens were divided into three groups with four vaginal specimens. The first group was obtained in the folicular phase; those of the second in the postovulatory phase and, finally, the last group corresponded to the secretory phase.

An Electron-Microscope Study of the Cytoplasmic Inclusions in the Neurones of Locusta Migratoria

1962 ◽  
Vol s3-103 (62) ◽  
pp. 147-153
Author(s):  
DOREEN E. ASHHURST ◽  
J. A. CHAPMAN
Keyword(s):  
Endoplasmic Reticulum ◽  
Electron Microscope ◽  
Microscope Study ◽  
Electron Microscope Study ◽  
Locusta Migratoria ◽  
Cytoplasmic Inclusions ◽  
Double Membrane

The cytoplasmic inclusions of the neurones of adult Locusta migratoria have been examined in the electron microscope. The mitochondria are easily recognized by their cristae and outer double membranes. Electron-dense inclusions, also with an outer double membrane but possessing numerous closely spaced internal lamellae in various orientations, are probably small lipochondria. Larger and more diffuse inclusions comprising crescent-shaped aggregates of loosely packed parallel lamellae and vesicles are present; the possible significance of these larger inclusions is discussed. A system of numerous small vesicles distributed throughout the cytoplasm makes up the endoplasmic reticulum.

scholarly journals AN ELECTRON MICROSCOPE STUDY OF YOLK FORMATION DURING OOGENESIS IN LEBISTES RETICULATUS GUPPYI

1966 ◽  
Vol 28 (2) ◽  
pp. 209-232 ◽  
Author(s):  
Michael J. Droller ◽  
Thomas F. Roth
Keyword(s):  
Endoplasmic Reticulum ◽  
Electron Microscope ◽  
Microscope Study ◽  
Electron Microscope Study ◽  
Structural Changes ◽  
Extracellular Material ◽  
Yolk Formation ◽  
Selective Uptake ◽  
Lebistes Reticulatus

The present investigation describes the fine structural changes that occur during proteid yolk formation in the developing oocytes of the guppy (Lebistes reticulatus), an ovoviviparous teleost. These changes suggest the operation of a number of different intra- and extraoocyte processes that may account for the synthesis and deposition of the proteid yolk. Early in oogenesis, the egg's Golgi systems proliferate and begin to disclose an electron-opaque content. Numerous 70-mµ diameter vesicles apparently pinch off from the Golgi systems, transport this material through the egg, and probably then fuse to form a crenate, membrane-limited yolk droplet. At the same time, the rough-surfaced endoplasmic reticulum accumulates a flocculent substance that differs in appearance from the Golgi content. Smooth vesicles, presumably derived from the ER, then coalesce to form a second type of intraoocyte yolk droplet. These dissimilar, separately derived droplets subsequently fuse, thus combining the materials that constitute the intraoocyte contribution to the proteid yolk. Somewhat later in development, the egg appears to ingest extracellular material via 75-mµ diameter bristle-coated micropinocytotic pits and vesicles. These structures apparently fuse to form tubules which then coalesce into large yolk droplets. At a later stage, bristle-coated micropinocytotic vesicles of 100 mµ diameter presumably take up a material that is then probably immediately deposited into a second type of proteid yolk droplet. It is postulated that these two different micropinocytotic structures are specifically involved with the selective uptake of dissimilar extracellular proteid materials.

scholarly journals APPLICATIONS OF FREEZE-SUBSTITUTION TO ELECTRON MICROSCOPE STUDIES OF INVERTEBRATE OOCYTES

1961 ◽  
Vol 9 (4) ◽  
pp. 785-798 ◽  
Author(s):  
Lionel I. Rebhun
Keyword(s):  
Endoplasmic Reticulum ◽  
Electron Microscope ◽  
Freeze Substitution ◽  
Ice Crystal ◽  
Considerable Similarity ◽  
Golgi Bodies ◽  
Substitution Process ◽  
Present Technique ◽  
Lead Hydroxide ◽  
Inner Light

A modified freeze-substitution process is described which gives a low percentage (less than 5 per cent) of preparations of invertebrate eggs which appear to be ice crystal-free at the resolution of the electron microscope. The mitochondria show no membranes in these preparations but can be recognized by internal spaces with the size and the distribution of the cristae. The Golgi bodies resemble those seen with diffusion fixatives, but the limiting membranes are here double; that is, they appear to be a triple-layered sandwich with two outer dark approximately 25A layers and an inner light layer of the same thickness. The endoplasmic reticulum is clearly present and resembles that seen with diffusion fixatives. Here again, the limiting membranes are double with the same dimensions as those in the Golgi bodies. The membranes of the Golgi bodies and ER are seen after permanganate but not lead hydroxide staining. The hyaloplasm (or "cell sap") is crowded with 150 to 200A particles and these are also seen lining the ER membranes. In general, the structures as seen with the present technique show considerable similarity to those seen with diffusion fixatives.

scholarly journals AN ELECTRON MICROSCOPE STUDY OF THE ENDOPLASMIC RETICULUM IN NEWT NOTOCHORD CELLS AFTER DISTURBANCE WITH ULTRASONIC TREATMENT AND SUBSEQUENT REGENERATION

1964 ◽  
Vol 20 (1) ◽  
pp. 175-183 ◽  
Author(s):  
G. G. Selman ◽  
A. Jurand
Keyword(s):  
Electron Microscopy ◽  
Endoplasmic Reticulum ◽  
Electron Microscope ◽  
Light Microscopy ◽  
Ultrasonic Treatment ◽  
Electron Microscope Study ◽  
Triturus Alpestris ◽  
Notochord Cells ◽  
Parallel Arrays ◽  
Subsequent Regeneration

Ultrasonic treatment of the tails of Triturus alpestris tadpoles, at intensities of 8 to 15 watts/cm2, at 1 megacycle/sec., for 5 minutes, disrupted the epidermis and caused pycnosis in individual cells of the muscle and neural tube, but caused no damage to the notochord that could be detected by light microscopy. Electron microscopy showed that this ultrasonic treatment disordered nearly all the endoplasmic reticulum (ER) of the notochord cells into irregularly rounded vesicles, but within 3 hours after treatment some parallel arrays of normal endoplasmic reticulum were seen near, and continuous with, the outer nuclear membrane. In addition, a re-ordering of the previously disordered ER took place throughout the cytoplasm, in some cases. A classification was made of the state of the ER as shown in electron micrographs of material fixed immediately, 3, and 24 hours after treatment. This showed that more than half the total endoplasmic reticulum in notochord cells was normal again by 24 hours after treatment.

The Connective-Tissue Sheath of the Nervous System of Locusta migratoria: an Electron Microscope Study

1961 ◽  
Vol s3-102 (60) ◽  
pp. 463-467
Author(s):  
DOREEN E. ASHHURST ◽  
J. A. CHAPMAN
Keyword(s):  
Endoplasmic Reticulum ◽  
Nervous System ◽  
Electron Microscope ◽  
Connective Tissue ◽  
Electron Microscope Study ◽  
Locusta Migratoria ◽  
Inner Surface ◽  
Connective Tissue Sheath ◽  
Cellular Layer ◽  
Sheath Cells

The sheath is composed of an outer non-cellular layer, the neural lamella, and an inner layer of sheath cells. The neural lamella possesses a large number of collagen fibrils arranged in layers with differing orientations. The sheath cells are flattened on the inner surface of the lamella and the cytoplasm contains lipochondria, mitochondria, and small amounts of endoplasmic reticulum.

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