scholarly journals A CYTOLOGICAL STUDY OF THE CENTRIFUGED WHOLE, HALF, AND QUARTER EGGS OF THE SEA URCHIN ARBACIA PUNCTULATA

1970 ◽  
Vol 47 (3) ◽  
pp. 711-733 ◽  
Author(s):  
Everett Anderson
Keyword(s):  
Lipid Droplets ◽  
Sea Water ◽  
Cytological Study ◽  
Germinal Vesicle ◽  
The Other ◽  
Annulate Lamellae ◽  
Cortical Granules ◽  
Clear Zone ◽  
Arbacia Punctulata ◽  
Peripheral Position

While the ooplasmic components of centrifuged eggs of Arbacia punctulata do not stratify in homogeneous layers, we have obtained the following strata beginning with the centripetal end: lipid droplets, pronucleus, clear zone, mitochondria, yolk, and pigment. Whereas mitochondria may be found mingled with yolk bodies, we have never observed lipid droplets nor pigment bodies among any of the other inclusions. The so-called clear zone contains a heterogeneous population of inclusions: annulate lamellae, heavy bodies, Golgi complexes, and rod-containing vacuoles. The peripheral cortical granules of immature (germinal vesicle stage) and of mature eggs are not dislodged from the cortical ooplasm with the centrifugal force utilized. When the eggs are treated with urethane, prior to centrifugation, the cortical granules of mature eggs abandon their peripheral position. Further centrifugation of the initially stratified eggs produces nucleated and nonnucleated halves and the centrifugation of the halves results in quarters. The cytology of the halves and quarters is discussed. The halves and quarters have been activated with either sperm or hypertonic sea water. With the exception of the nucleated halves, we were unable to obtain plutei larvae from the other fractions (red halves and quarters). We believe that the lack of development of the various fragments is a function of the balance of particular inclusions necessary for differentiation.

scholarly journals Electron Microscopy of the Centrifuged Sea Urchin Egg, with a Note on the Structure of the Ground Cytoplasm

1960 ◽  
Vol 7 (1) ◽  
pp. 135-142 ◽  
Author(s):  
Paul R. Gross ◽  
Delbert E. Philpott ◽  
Sylvan Nass
Keyword(s):  
Sea Urchin ◽  
Composite Structures ◽  
Annulate Lamellae ◽  
Cortical Granules ◽  
Clear Zone ◽  
Arbacia Punctulata ◽  
Large Numbers ◽  
Sea Urchin Egg ◽  
Size Number

Centrifuged, unfertilized eggs of the sea urchin, Arbacia punctulata, have been studied with the electron microscope. Subcellular particles were stratified by centrifuging living cells, known to be normally fertilizable, for five minutes at 3,000 g. The layered subcellular particles, including cortical granules, 16 mµ RNP particles, pigment, yolk, mitochondria, and oil droplets, possess characteristic ultrastructural features by which they may be identified in situ. The clear zone contains 16 mµ particles, most of them freely dispersed, scattered mitochondria, and a few composite structures made up of annulate lamellae in parallel layers or in association with dense, spherical aggregates of the RNP particles. Free 16 mµ particles are found, in addition, throughout the cell, in the interstices between the stratified larger particles. They show a tendency to form ramifying aggregates resulting from certain types of injury to the cell. A few vesicular structures, found mainly in the clear zone, have attached RNP particles, and appear to be related to the ER of tissue cells. Other vesicles, bounded by smooth membranes, are found throughout the cell. These are extremely variable in size, number, and distribution; their total number appears to depend upon conditions of fixation. It is suggested that limited formation of such structures is a normal property of the ground cytoplasm in this cell, but that fixed cells with very large numbers of smooth surfaced vesicles have produced the latter as a response to chemical injury. A model of the ground cytoplasm is proposed whose aim is to reconcile the rheological behavior of the living cell with the ultrastructural features observed.

scholarly journals A CYTOLOGICAL STUDY OF ARTIFICIAL PARTHENOGENESIS IN THE SEA URCHIN ARBACIA PUNCTULATA

1970 ◽  
Vol 47 (1) ◽  
pp. 140-158 ◽  
Author(s):  
Martin I. Sachs ◽  
Everett Anderson
Keyword(s):  
Endoplasmic Reticulum ◽  
Sea Urchin ◽  
Nuclear Division ◽  
Annulate Lamellae ◽  
Cortical Granules ◽  
Smooth Variety ◽  
Mitotic Apparatus ◽  
Arbacia Punctulata ◽  
The Matrix ◽  
Cell Embryo

Eggs of the sea urchin Arbacia punctulata were artificially activated with hypertonic seawater. The artificially activated eggs undergo the cortical reaction which is not distinguished by a wavelike progression as in the case of inseminated eggs. The cortical granules are released at random loci at the surface of the egg and result in spaces separated by large cytoplasmic projections. Unreacted cortical granules and ribosomes are found within the matrix comprising the large cytoplasmic projections. No "fertilization cone" is formed. The subsequent release of additional cortical granules results in the formation of a continuous perivitelline space, 15 min following activation. 85 min postactivation, an organization of annulate lamellae, endoplasmic reticulum of the smooth variety, and microtubules around a centriole is observed prior to nuclear division. Before the breakdown of the nuclear envelope a streak stage is formed. The streak is composed of a central core of annulate lamellae and is encompassed by endoplasmic reticulum and vesicular components. Condensation of chromatin is followed by the establishment of the mitotic apparatus. Centrioles were not found in the mature egg; however, they are present after activation prior to the first nuclear division, in the four-cell embryo, multicellular embryo, and at blastula. Artificially activated eggs have been observed to develop to the pluteus stage in more than 50% of the eggs treated.

An ultrastructural study on the shark liver

1990 ◽  
Vol 48 (3) ◽  
pp. 512-513
Author(s):  
Masako Yamada ◽  
Yutaka Tanuma
Keyword(s):  
Portal Vein ◽  
Kupffer Cells ◽  
Ultrastructural Study ◽  
Lipid Droplets ◽  
Microscopic Level ◽  
The Other ◽  
Fish Stock ◽  
Structural Studies ◽  
Light Microscopic Level ◽  
Perfusion Fixation

Although many fine structural studies on the vertebrate liver have been reported on mammals, avians, reptiles, amphibians, teleosts and cyclostomes, there are no studies on elasmobranchii liver except one by T. Ito etal. (1962) who studied it on light microscopic level. The purpose of the present study was to as certain the ultrastructural details and cytochemical characteristics of normal elasmobranchii liver and was to compare with the other higher vertebrate ones.Seventeen Scyliorhinus torazame, one kind of elasmobranchii, were obtained from the fish stock of the Ueno Zoo aquarium, Ueno, Tokyo. The sharks weighing about 300-600g were anesthetized with MS-222 (Sigma), and the livers were fixed by perfusion fixation via the portal vein according to the procedure of Y. Saito et al. (1980) for 10 min. Then the liver tissues were immersed in the same fixative for 2 hours and postfixed with 1% OsO4-solution in 0.1 Mc acodylate buffer for one hour. In order to make sure a phagocytic activity of Kupffer cells, latex particles (0.8 μm in diameter, 0.05mg/100 g b.w.) were injected through the portal vein for one min before fixation. For preservation of lipid droplets in the cytoplasm, a series of these procedure were performed under ice cold temperature until the end of dehydration.

Induction of DNA replication in germinal vesicles and in nuclei formed in maturing mouse oocytes by 6-DMAP treatment

Zygote ◽  
1997 ◽  
Vol 5 (3) ◽  
pp. 213-217 ◽  
Author(s):  
J. Fulka ◽  
N.L. First ◽  
C. Lee ◽  
J. Fulka ◽  
R.M. Moor
Keyword(s):  
Dna Replication ◽  
Dna Synthesis ◽  
Germinal Vesicle ◽  
The Other ◽  
Immature Oocytes ◽  
Mouse Oocytes ◽  
Germinal Vesicles ◽  
Immature Mouse ◽  
Condensed Dna ◽  
Metaphase Ii Oocytes

SummaryImmature mouse oocytes (germinal vesicle stage, GV), oocytes at different stages during maturation (prometaphase to anaphase I) and matured oocytes (metaphase II arrested) were cultured in 6-dimethylaminopurine (6-DMAP)-supplemented medium also containing bromodeoxyuridine for the assessment of DNA replication in these cells. Immature oocytes remained arrested at the GV stage and DNA replication was never detected in them. On the other hand, oocytes at the prometaphase to anaphase-telophase I stages responded to 6-DMAP treatment by forming nuclei which synthesised DNA. Mature (metaphase II) oocytes did not respond to 6-DMAP and their chromatin remained condensed. DNA synthesis could even be induced in GV-staged oocytes, but only when they were fused to freshly activated oocytes and incubated in 6-DMAP-supplemented medium.

Part 2. The deeper structure of the Atlantic - Geological hypotheses and the earth's crust under the oceans

1954 ◽  
Vol 222 (1150) ◽  
pp. 341-348 ◽  
Keyword(s):  
Heat Flow ◽  
Recent Work ◽  
Sea Water ◽  
Volcanic Rocks ◽  
The Other ◽  
Ocean Floor ◽  
Peridotite Xenoliths ◽  
The Earth ◽  
Southern Rhodesia ◽  
Mohorovičić Discontinuity

Recent work has determined the depth of the Mohorovičić discontinuity at sea and has made it likely that peridotite xenoliths in basaltic volcanic rocks are samples of material from below the discontinuity. It is now possible to produce a hypothetical section showing the transition from a continent to an ocean. This section is consistent with both the seismic and gravity results. The possible reactions of the crust to changes in the total volume of sea water are dis­cussed. It seems possible that the oceans were shallower and the crust thinner in the Archean than they are now. If this were so, some features of the oldest rocks of Canada and Southern Rhodesia could be explained. Three processes are described that might lead to the formation of oceanic ridges; one of these involves tension, one compression and the other quiet tectonic conditions. It is likely that not all ridges are formed in the same way. It is possible that serpentization of olivine by water rising from the interior of the earth plays an important part in producing changes of level in the ocean floor and anomalies in heat flow. Finally, a method of reducing gravity observations at sea is discussed.

Fine structural observations on oocyte development in monogeneans

Parasitology ◽  
1976 ◽  
Vol 73 (1) ◽  
pp. 13-23 ◽  
Author(s):  
D. W. Halton ◽  
S. D. Stranock ◽  
Anne Hardcastle
Keyword(s):  
Meiotic Prophase ◽  
Species Differences ◽  
Ultrastructural Changes ◽  
Cell Periphery ◽  
Annulate Lamellae ◽  
Cellular Activity ◽  
Cortical Granules ◽  
Primary Oocyte ◽  
Nucleolar Volume ◽  
Oocyte Differentiation

SummaryThe ultrastructural changes accompanying oocyte differentiation in the ovaries of the monogeneans, Diclidophora merlangi, Diplozoon paradoxum and Calicotyle kröyeri have been described. In each case, oogenesis in the ovary proceeds as far as meiotic prophase in the primary oocyte. A three-stage sequence of development based on oocyte morphology is proposed: (1) Oogonia and early, immature primary oocytes are typically undifferentiated, with chromatin-laden nuclei occupying most of the cell volume. The cytoplasm contains small clumps of mitochrondria and unattached ribosomal aggregates. There is evidence of mitosis and, in later stages, meiotic prophase is indicated by the appearance of nuclear synaptonemal complexes. (2) Maturing primary oocytes are characterized by increased nucleolar volume associated with the production of RNA for export to the cytoplasm. An organized GER and Golgi apparatus are established and involved in the synthesis and packaging of membrane-limited cortical granules. Annulate lamellae and nucleolus-like bodies appear in the cytoplasm and, with development, the cells increase in size and, peripherally, become interdigitated. (3) Mature primary oocytes represent a resting phase when cellular activity is minimal. Golgi disappear and the ER fragments or becomes reduced in dimensions. Mitochondria and free ribo-somes are numerous and cortical granules move to the cell periphery. The cells separate and, when mature, are released from the ovary. There are minor species differences in oocyte ultrastructure and development.

The unreliability of mammalian glomerular markers in teleostean renal studies

1976 ◽  
Vol 64 (2) ◽  
pp. 369-378 ◽  
Author(s):  
K. W. Beyenbach ◽  
L. B. Kirschner
Keyword(s):  
Polyethylene Glycol ◽  
Urinary Bladder ◽  
Glomerular Filtration ◽  
Sea Water ◽  
The Other ◽  
Salmo Gairdneri ◽  
Renal Tubules ◽  
True Measure

1. The assumption that (3H) methoxy inulin, (14C) polyethylene glycol (PEG) and (125) iothalamate (glofil) are reliable volume and glomerular markers in teleosts was tested. 2. PEG occupied smaller volumes than inulin and glofil in sea-water-adapted Salmo gairdneri. Ureteral clearances of PEG were about 22% higher than those of inulin and glofil, and urine-to-plasma ratios were significantly greater for PEG than for the other two markers. 3. After introduction into the urinary bladder the three macro-molecules appeared in the plasma, PEG at the lowest rates. 4. These observations indicate that mammalian glomerular markers can penetrate the bladder and possibly the ureters and renal tubules. Therefore, their clearances may not give a true measure of glomerular filtration rates in teleosts.

Oocyte maturation: aberrant post-fusion responses of the rabbit primary oocyte to penetrating spermatozoa

1979 ◽  
Vol 39 (1) ◽  
pp. 1-12
Author(s):  
M. Berrios ◽  
J.M. Bedford
Keyword(s):  
Anterior Part ◽  
Light And Electron Microscopy ◽  
Germinal Vesicle ◽  
Sperm Chromatin ◽  
Fallopian Tubes ◽  
Cortical Granules ◽  
Germinal Vesicle Breakdown ◽  
Acrosomal Membrane ◽  
Primary Oocyte ◽  
Inner Acrosomal Membrane

Primary oocytes cannot be fertilized normally; they begin to develop this capacity as meiosis resumes. To elucidate the changes involved in acquisition of their fertilizability, rabbit primary oocytes displaying a germinal vesicle (GV oocytes) were placed in Fallopian tubes inseminated previously with spermatozoa, recovered 2–5 h later and examined by light and electron microscopy. At least 4 aspects of GV oocyte/sperm interaction were abnormal. Although the vestments and oolemma seem normally receptive to spermatozoa, fusion with the oolemma of the primary oocyte did not elicit exocytosis of cortical granules, and consequently multiple entry of spermatozoa into the ooplasm was common. Secondly, the GV oocyte cortex failed to achieve a normal englufment of the anterior part of the sperm head. It sank into the ooplasm capped by only a small rostral vesicle or left the stable inner acrosomal membrane as a patch in the oolemma. Only rarely then was there significant dispersion of the sperm chromatin, and this remained surrounded by nuclear envelope. The persistence of this envelope constitutes a further aberrant feature, for it disappears immediately in secondary oocytes and was absent in primary oocytes in which germinal vesicle breakdown had occurred. The results are discussed with particular reference to current ideas about male pronucleus formation.

Structural hybridity and supernumerary chromosomes in a diploid Tradescantia hirsuticaulis

1975 ◽  
Vol 53 (5) ◽  
pp. 456-465 ◽  
Author(s):  
C. C. Chinnappa
Keyword(s):  
Reciprocal Translocation ◽  
Cytological Study ◽  
B Chromosomes ◽  
The Other ◽  
Meiotic Pairing ◽  
Structural Hybridity ◽  
Supernumerary Chromosomes

Cytological study of a diploid (2n = 12) population of Tradescantia hirsuticaulis Small from Stone Mountain, Georgia, revealed striking variation in four plants growing in a cluster, indicating that they constitute different genotypes. The occurrence of B chromosomes, fragments, and aneusomaty in the plants is associated with structural hybridity in the chromosomes. Two plants were homozygotes with simple meiotic pairing, one was heterozygous for a reciprocal translocation, and the other was a heterozygote for two interchanges as well as for inversions. The behavior and the origin of B chromosomes, fragments, and structural hybridity are discussed.

scholarly journals THE EXTRACELLULAR RELEASE OF ECHINOCHROME

1946 ◽  
Vol 29 (5) ◽  
pp. 267-275 ◽  
Author(s):  
Herbert Shapiro
Keyword(s):  
Sea Urchin ◽  
Sea Water ◽  
Potassium Content ◽  
Red Pigment ◽  
Anaerobic Conditions ◽  
Outward Diffusion ◽  
Arbacia Punctulata ◽  
Extracellular Release

A study was made of the diffusion of the red pigment echinochrome from the eggs of the sea urchin, Arbacia punctulata, into sea water. Unfertilized eggs retained their pigment, over periods of hours. Outward diffusion of pigment from unfertilized eggs normally is entirely negligible, or does not occur at all. Enchancing the calcium or potassium content of the artificial sea water (while retaining isosmotic conditions) did not induce pigment release. Under anaerobic conditions, unfertilized eggs release pigment in small quantities. Fertilization alone brings about echinochrome release. Fertilized eggs invariably released pigment, whether in normal sea water, or sea water with increased calcium or potassium. This diffusion of the pigment began during the first cleavage, possibly soon after fertilization. The pigment release is not a consequence solely of the cell's permeability to echinochrome (or chromoprotein, or other pigment combination) but is preceded by events leading to a release of echinochrome from the granules in which it is concentrated within the cell. These events may be initiated by activation or by anaerobiosis. The phenomenon was not due to cytolysis.

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