A Feulgen technique for identification of cucumber chromosomes

1983 ◽  
Vol 39 (10) ◽  
pp. 1155-1156 ◽  
Author(s):  
C. Ramachandran ◽  
R. A. Pai ◽  
V. S. Seshadri
Keyword(s):  
1987 ◽  
Vol 65 (2) ◽  
pp. 296-303 ◽  
Author(s):  
Sharon A. MacLean ◽  
Carol M. Morrison ◽  
Robert A. Murchelano ◽  
Sherie Everline ◽  
Joyce J. Evans

Results of light and electron microscopic examinations of cysts of unknown etiology (CUEs) occurring in the gills of Atlantic mackerel, red hake, white hake, cod, haddock, and silver hake are presented. CUEs were found also in gills and viscera of winter flounder, Atlantic croaker, spot, windowpane flounder, and sand lance. CUEs measured 150–400 μm in diameter and consisted of an external fibrous cuticle, usually a thick median band, and a central core that frequently contained eosinophilic vesicles. Structures resembling mitochondria were found in the band and in vesicles of the core, but no other organelles were apparent. Cytochemical staining and ultramicroscopy revealed aggregates of glycogen in the core ground substance; no structural components were stained with Sudan black B or by the Feulgen technique. Extensive encapsulation of CUEs by fibroblasts was typical. Of 717 mackerel examined, 76.8% had CUEs in the gills; numbers ranged from 1 to 353 per fish. The prevalence and intensity of occurrence of CUEs increased with the age of the mackerel.


1938 ◽  
Vol s2-80 (318) ◽  
pp. 293-319
Author(s):  
MARGARET I. DANIELS

A. Three gregarine species are found to inhabit the mid-gut of the mealworm larvae used: Gregarina cuneata Stein, Gregarina polymorpha Hamm, and Gregarina steini Berndt. The often described Steinina ovalis is probably seldom or never found. They live only in the mid-gut of larvae. They are never found in pupal or adult forms. Gregarines have been seen moving when in a stratified condition. B. The gregarine cytoplasm has five important inclusions, each having a characteristic position in a centrifuged animal (Text-fig. 2). 1. Paraglycogen.--This gives a dark brown colour with iodine, a pinkish general colour with the acid fuchsin of the Feulgen technique, and often a red colour with Bauer's reaction. It occupies the centrifugal pole of the centrifuged cell and is in the form of disc-like granules of varying size. 2. In young centrifuged Gregarina steini chromidial granules are seen in the paraglycogen area, and have, therefore, approximately the same specific gravity. They arise by karyosomic budding with the subsequent extrusion of these buds into the cytoplasm. They stain with iron alum haematoxylin, like the karyosome, and both give a negative result with the Feulgen test for thymonucleic acid. They probably correspond to Joyet-Lavergne's ‘albuminoid reserves’, but do not have the mitochondrial‘cap’ he describes. 3. Mitochondria.--These are usually granular, but sometimes rod-like. They are seen between the ‘alveoli’ formed by the paraglycogen granules. They lie distally to the paraglycogen in a centrifuged parasite; they stain by the iron alum haematoxylin long method, after Benoit, Champy, or Altmann fixation, also with Altmann's fuchsin picric acid stain and the Bensley Cowdry modification of it. 4. The Nucleus is karyosomic, and the karyosome is moved to the centrifugal pole by pressure as is the nucleolus of metazoan cells. The nucleus shows budding of the karyosome. There is plasmatic as well as chromatic material in the karyosome, as shown by centrifuging. The nucleus gives a negative result with Feulgen's nuclear reaction, but chromatin may exist in a very dispersed condition. 5. Golgi Material.--This lies at the centripetal end of the nucleus. It is best shown by Weigl fixation. The large and regular Golgi elements are slightly heavier than the granular Golgi material, which may be compared with that of young oocytes. 6. Fatty Material lies at the extreme centripetal pole of the cell, in globules of varying size. It becomes brown or black after treatment with osmium tetroxide, and vivid cherry red with Sudan IV. It gives a negative result with the Schultz reaction for cholestrol. C. Large globules are seen in the protomerite of Gregarina steini , eosinophile, sometimes fuchsinophile, and also staining with methylene blue. These move towards the centrifugal pole. Methylene blue preparations show blue granules among the paraglycogen granules in the centrifuged animal. They are remarkably resistant to dilute sulphuric acid. They are possibly allied to volutin or chromidia. Tests for the presence of Vitamin C yielded negative results. Only the inclusions of the gregarines in the gut lumen were studied, and the complete life-cycles of the species were not followed out.


Parasitology ◽  
1955 ◽  
Vol 45 (3-4) ◽  
pp. 421-425 ◽  
Author(s):  
H. N. Ray ◽  
B. Dasgupta

1. NR bodies show special affinity for neutral red. They are rounded or irregular in outline, measuring 0·25–12·5µ in diameter.2. In fixed preparations NR bodies appear as spherical and vacuolated structures.3. RNA is present in abundance in mature NR bodies, but while DNA is present in variable amount, the Feulgen technique shows that in their very young stage NR bodies are rich in DNA.4. Glycogen is absent from the NR bodies, but Hale's technique provides evidence that the hyaluronic acid type of polysaccharide is present in them.5. By Gomori's modified technique the presence of alkaline phosphatase in the NR body was demonstrated.6. The mature NR bodies multiply by a process of budding. Small buds or spherules rich in DNA infect fresh spermatogonial cells, the latter being converted into the ‘pathological cells’ of Hertig.


1967 ◽  
Vol 45 (4) ◽  
pp. 447-450 ◽  
Author(s):  
Ramesh Maheshwari ◽  
A. C. Hildebrandt ◽  
P. J. Allen

Urediospores of Uromyces phaseoli var. typica (Pers.) Wint. race 32 Arth. germinated on mineral oil – nitrocellulose membranes and sequentially developed appressoria, vesicles, and infection hyphae. The nuclear behavior during in vitro differentiation of infection structures was studied by use of the Feulgen technique. The two urediospore nuclei divided in the germ tube before the formation of appressorium. This was followed by a second division of the four daughter nuclei in the appressorium, and occasionally by a third division of the eight nuclei in the vesicle and infection hypha. Haustorial mother cells were formed in infection hyphae in vitro and contained from two to five nuclei. In contrast, nuclear division did not occur in germ tubes where growth continued linearly. Infection structures that developed in vitro resembled those produced during infection of the host by urediospores of other species of rust fungi.


1961 ◽  
Vol 10 (3) ◽  
pp. 353-359 ◽  
Author(s):  
G. W. Salisbury ◽  
W. J. Birge ◽  
L. de la Torre ◽  
J. R. Lodge

The Feulgen-DNA content of sperm cells from 5 bulls was studied by means of microspectrophotometry after storage at 5°C for 2, 3, 5, and 10 days in a yolk-citrate diluent permitting slow aerobic metabolism. A subsample of sperm cells from each bull was subjected to the Feulgen technique on each of the storage days selected. The cells sampled on each of these days received a standard 12 minute, 60°C hydrolysis. Absorption measurements at 546 mµof the individual cells indicated a marked progressive decrease in the Feulgen-DNA content of the stored spermatozoa. The loss of 30 per cent of the initial DNA at the end of 5 days' storage was highly significant statistically. This decrease approximately parallels the known decrease in fertility of stored sperm cells, as well as the increase in apparent embryonic mortality resulting from the use of similarly aged spermatozoa for artificial insemination.


Parasitology ◽  
1965 ◽  
Vol 55 (1) ◽  
pp. 117-125 ◽  
Author(s):  
R. A. R. Gresson

While some variation of detail may be found in different species of the hermaphroditic Digenea, the process of spermatogenesis conforms to a common plan throughout the group. There is divergence of opinion concerning the interpretation of the structure of the ripe spermatozoon.In the testis of a young animal, primary, secondary and tertiary spermatogonia are present. The tertiary spermatogonia divide to give a group of eight primary spermatocytes that undergo the first division of the meiotic phase to form sixteen secondary spermatocytes. As a result of the second division of the meiotic phase, the sixteen secondary spermatocytes give a group of thirty-two spermatids that through a complicated series of changes are transformed into spermatozoa. During spermateleosis much of the cytoplasm of the late spermatid is sloughed off.Recent research, including the application of the Feulgen technique, the examination of living material, and electron microscopy, supports the view that the ripe spermatozoon is composed of an elongate head, and a flagellum. The head, with the exception of its external sheaths, consists of nuclear material.The flagellum of the sperm of Fasciola hepatica is Feulgen-negative and is composed of a proximal and a distal region. Its proximal part is provided with two axial filaments, a middle fibril and an external sheath. The axial filaments and the middle fibril are continued into the distal region where the external sheath appears to be absent. The external sheath of the flagellum of the sperm of Haematoloechus ( = Ostiolum) medioplexus is said to be composed of thirty-six fibrils. Claims that the flagellum of some digeneans contains a centriole, a middle-piece, and mitochondria have not so far been substantiated by means of electron microscopy.


1963 ◽  
Vol 19 (2) ◽  
pp. 285-291 ◽  
Author(s):  
M. R. Loran ◽  
T. T. Crocker

Sprague-Dawley rats that had been subjected 2 months previously to partial resection (10 per cent) of the small intestine and an equal number of control rats were injected with tritiated thymidine and sacrificed at intervals during the subsequent 16 hours. Segments of duodenum, jejunum and ileum were prestained by the Feulgen technique and radioautographed. The proportion of crypt cells bearing labeled nuclei, the percentage of labeled crypt cells in mitosis and the appearance of labeled crypt cells on the villi were determined. Comparison of control and resected rats showed that (a) the proportion of intestinal crypt cells incorporating thymidine was considerably greater and uniformly high throughout the shortened intestine, (b) the life cycle of crypt cells was slightly reduced, and was uniform throughout the shortened intestine, and (c) the time during which cells were retained in crypts was markedly reduced. On the basis of persistent, generalized increase in the production of crypt cells, and on prior evidence that the epithelial cells of shortened intestine continue to have a brief life span and evidence of metabolic immaturity, the existence of a humoral factor, tentatively called "intestinal epithelial growth hormone," is postulated.


1957 ◽  
Vol s3-98 (44) ◽  
pp. 493-498
Author(s):  
R.A. R. GRESSON

The stages of spermateleosis and the structure of the spermatozoon of Fasciola hepatica were studied in smears of fixed material and in preparations of living tissue examined under phase-contrast microscopy. Smears were fixed in Bouin's picro-formol and in Flemming without acetic. Smears were also prepared according to the Feulgen technique. The nucleus of the late spermatid undergoes elongation and grows out from the distal end of the cell. An extension of cytoplasm gives rise to the sperm-tail or flagellum. The spermatozoon becomes free of the greater part of the cytoplasm of the spermatid; the latter remains as a residual mass. The spermatozoon consists of a nucleus and a flagellum. The latter is probably composed of an axial filament surrounded by a thin sheath of cytoplasm.


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