Oocyte Developmental Stages and its Relationship with the Zona Layers During Vitellogenesis in the Asian Striped Catfish Mystus vittatus (Bloch, 1794)

The present study reports successful induced breeding of endangered striped dwarf catfish Mystus vittatus and its different embryonic and larval developmental stages. Three different doses of PG were tested, viz. 17, 15 and 13 mg PG/kg body weight for female and 14, 12 and 10 mg PG/kg body weight for male with maintaining (1:1) male and female ratio. The hormone doses 13 mg/kg for female and 10 mg/kg for male provided the best result i.e. 91.33±2.08% fertilization and 85.00±2% hatching rates. Mean survival percentage of the spawns up to 21 days was 8.00±1%. The fertilized eggs were found to be transparent, demersal, spherical, adhesive and brownish in colour and first cleavage took place within 35-40 min post-fertilization at 29.56± 0.25oC. Hatching took place at 24 h. after fertilization. Newly hatched larvae were 3-4 mm in length and slender, transparent and the yolk sac oval in shape. Anus was situated at almost mid ventrally. Larvae started to feed at 48-72 h post-hatching. DOI: http://dx.doi.org/10.3329/ralf.v1i1.22376 Res. Agric., Livest. Fish.1(1): 127-136, Dec 2014

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Correlated Studies of Cellular Interactions Using TEM, Freeze Etching, and SEM

Proceedings, annual meeting, Electron Microscopy Society of America ◽

10.1017/s042482010005161x ◽

1974 ◽

Vol 32 ◽

pp. 320-321

Author(s):

J. P. Revel

Keyword(s):

Developmental Stages ◽

Three Dimensional ◽

Cell Movement ◽

Cellular Interactions ◽

Serial Sections ◽

Cell Sheets ◽

Freeze Etching ◽

Early Developmental

Movement of individual cells or of cell sheets and complex patterns of folding play a prominent role in the early developmental stages of the embryo. Our understanding of these processes is based on three- dimensional reconstructions laboriously prepared from serial sections, and from autoradiographic and other studies. Many concepts have also evolved from extrapolation of investigations of cell movement carried out in vitro. The scanning electron microscope now allows us to examine some of these events in situ. It is possible to prepare dissections of embryos and even of tissues of adult animals which reveal existing relationships between various structures more readily than used to be possible vithout an SEM.

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Electron investigations of rhabdovirus-like particles in mexican bean beetles and crickets

Proceedings, annual meeting, Electron Microscopy Society of America ◽

10.1017/s0424820100082753 ◽

1978 ◽

Vol 36 (2) ◽

pp. 378-379

Author(s):

J. R. Adams ◽

G. J Tompkins ◽

A. M. Heimpel ◽

E. Dougherty

Keyword(s):

Biological Control ◽

Integrated Pest Management ◽

Pest Management ◽

Developmental Stages ◽

Management Program ◽

Acheta Domesticus ◽

Epilachna Varivestis ◽

House Cricket ◽

Similar Morphology ◽

Bean Beetle

As part of a continual search for potential pathogens of insects for use in biological control or on an integrated pest management program, two bacilliform virus-like particles (VLP) of similar morphology have been found in the Mexican bean beetle Epilachna varivestis Mulsant and the house cricket, Acheta domesticus (L. ).Tissues of diseased larvae and adults of E. varivestis and all developmental stages of A. domesticus were fixed according to procedures previously described. While the bean beetles displayed no external symptoms, the diseased crickets displayed a twitching and shaking of the metathoracic legs and a lowered rate of activity.Examinations of larvae and adult Mexican bean beetles collected in the field in 1976 and 1977 in Maryland and field collected specimens brought into the lab in the fall and reared through several generations revealed that specimens from each collection contained vesicles in the cytoplasm of the midgut filled with hundreds of these VLP's which were enveloped and measured approximately 16-25 nm x 55-110 nm, the shorter VLP's generally having the greater width (Fig. 1).

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The Fine Structure of the Sheath of Volvox Carteri f. Weismannia

Proceedings, annual meeting, Electron Microscopy Society of America ◽

10.1017/s0424820100079231 ◽

1977 ◽

Vol 35 ◽

pp. 346-347

Author(s):

Regina Birchem

Keyword(s):

Developmental Stages ◽

Ruthenium Red ◽

Sulfated Polysaccharides ◽

Volvox Carteri ◽

High Voltage Electron Microscopy ◽

Ultrastructural Studies ◽

Voltage Electron ◽

Sheath Formation ◽

And Inversion ◽

Sheath Material

Spheroids of the green colonial alga Volvox consist of biflagellate Chlamydomonad-like cells embedded in a transparent sheath. The sheath, important as a substance through which metabolic materials, light, and the sexual inducer must pass to and from the cells, has been shown to have an ordered structure (1,2). It is composed of both protein and carbohydrate (3); studies of V. rousseletii indicate an outside layer of sulfated polysaccharides (4).Ultrastructural studies of the sheath material in developmental stages of V. carteri f. weismannia were undertaken employing variations in the standard fixation procedure, ruthenium red, diaminobenzidine, and high voltage electron microscopy. Sheath formation begins after the completion of cell division and inversion of the daughter spheroids. Golgi, rough ER, and plasma membrane are actively involved in phases of sheath synthesis (Fig. 1). Six layers of ultrastructurally differentiated sheath material have been identified.

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Localization of acid phosphatases in root cap of rice plant

Proceedings, annual meeting, Electron Microscopy Society of America ◽

10.1017/s0424820100085423 ◽

1991 ◽

Vol 49 ◽

pp. 224-225

Author(s):

Y. R. Chen ◽

Y. F. Huang ◽

W. S. Chen

Keyword(s):

Rice Plant ◽

Developmental Stages ◽

Uranyl Acetate ◽

Root Cap ◽

Plant Tissues ◽

Acid Phosphatases ◽

Root Tips ◽

Buffer Solution ◽

Cacodylate Buffer ◽

Ethanol Series

Acid phosphatases are widely distributed in different tisssues of various plants. Studies on subcellular localization of acid phosphatases show they might be present in cell wall, plasma lemma, mitochondria, plastid, vacuole and nucleus. However, their localization in rice cell varies with developmental stages of cells and plant tissues. In present study, acid phosphatases occurring in root cap are examined.Sliced root tips of ten-day-old rice(Oryza sativa) seedlings were fixed in 0.1M cacodylate buffer containing 2.5% glutaraldehyde for 2h, washed overnight in same buffer solution, incubated in Gomori's solution at 37° C for 90min, post-fixed in OsO4, dehydrated in ethanol series and finally embeded in Spurr's resin. Sections were doubly stained with uranyl acetate and lead citrate, and observed under Hitachi H-600 at 75 KV.

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