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J C Stockert

Publications and source records attributed to J C Stockert.

At least 127 records · Page 7Linked to original sources

Localization of the synaptonemal complex under the light microscope.

The use of osmium tetroxide fixation followed by postreatment with p-phenylenediamine gives an opportunity of locating the synaptonemal complex (SC) under the light microscope in mouse testes and Allium cepa anthers. When semi-thin sections from these materials were observed under phase contrast optics or dark field microscopy, fine threads in the pachytene nuclei were clearly visible. Post-staining of semi-thin sections with ammoniacal silver increased the contrast of the SC and allowed for observations using a bright field illumination. Ultrathin sections of osmium tetroxide/p-phenylenediamine treated material showed that, under the electron microscope, this technique stains preferentially elements of the synaptonemal complex, while the surrounding chromatin remains unstained.

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Toluidine blue staining on Epon semithin sections: effect of an oil differentiation.

Semithin sections from glutaraldehyde-osmium fixed, Epon embedded tissues were stained by alkaline toluidine blue and subjected to prolonged oil treatment. This procedure resulted in progressive bleaching of sections, while a few cell structures remained highly stained. The possible mechanism of this "differentiation" effect induced by the oil treatment is briefly analyzed.

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Observations on the nucleolar staining by ethanolic phosphotungstic acid.

In addition to the already known reactivity of heterochromatin masses and synaptonemal complexes for ethanolic phosphotungstic acid, nucleoli from Sertoli cells show a preferential electron microscopic staining of the pars fibrosa. This ultrastructural pattern can be correlated with intranucleolar differentiations observed in light microscopy after staining of semithin sections with Unna's polychrome blue.

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Osmium tetroxide/p-phenylenediamine staining of nucleoli and Balbiani Rings in Chironomus salivary glands.

This paper deals with the application of the osmium tetroxide fixation followed by p-phenylenediamine treatment to salivary gland cells from Chironomus larvae. After this procedure, cytoplasm, nucleoli and Balbiani rings show a high degree of staining both in light and electron microscopy, while chromatin remains unstained. Ethanol fixation followed by osmium tetroxide/p-phenylenediamine does not modify the above mentioned staining pattern. Under these conditions, extractive procedures for lipids do not affect the osmiophilia of nucleoli and Balbiani rings, while RNase or trichloroacetic acid treatment decreaes the staining degree of these structures. In osmium tetroxide/p-phenylenediamine treated salivary glands, the highest contrast within nuclei is seen to occur in the pars granulosa from normal or segregated nucleoli, as well as in Balbiani ring granules, which appear either as hollow granules or with a bipartite or horseshoe-like structure.

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Puffing patterns during the fourth larval instar in Chironomus pallidivittatus salivary glands.

The puffing pattern of polytene chromosomes in salivary glands from Chironomus pallidivittatus larvae and prepupae has been studied in glutaraldehyde-acetic acid fixed, lactic acid flattened preparations. Some observations were also made on F1 hybrid species C. pallidivittatus X C. tentans. Concerning the situation of puffing in Balbiani rings (BR), 2.783 chromosomes IV from 188 animals were scored. In standard 4th instar larvae, BR2 appears expanded, BR3 smaller but not collapsed and BRI either reduced of collapsed. During the first days following the red-head stage, which signals the beginning of the 4th instar, larvae show a large BR1; later it reduces and tends to collapse. At the end of the 4th instar, prepupae again may present an expanded BR1. On the contrary, the size of BR2 and BR3 remains unchanged from the red-head stage to the prepupa. A variable accumulation of droplets has been observed to occur in BR2 and BR1 from dated larvae and prepupae.--A characteristic pattern of puffing was found in prepupae, which consisted in the appearance of conspicuous puffs at regions I-6B, I-7B, I-7B, I-18C, III-9B and IV-4B. Puffs at I-2B, I-3B, I-9A,I-11C,II-4A, and IV-4B were observed during most of the 4th larval instar, as well as in late larvae and prepupae. Among all these puffs, those at I-7B, I-9A, I-17B, and IV-4B frequently showed variable amounts of droplets.

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Uranyl-EDTA-hematoxylin: a new selective staining technique for nucleolar material.

This paper deals with the visualization of nuclear structures in glutaraldehyde fixed, acetic acid flattened preparations from Chironomus salivary glands, by means of an uranyl mordanting followed by hematoxylin staining. Under these conditions all the nuclear structures (bands, Balbiani rings, and nucleoli) were deeply stained. Treatment with 0.1 M EDTA for at least 30 sec after uranyl mordanting completely prevents the following hematoxylin staining in all the structures but the nucleolus. With increased EDTA extraction times (60-90 sec) the central region (composed of pars fibrosa) in spontaneously or experimentally segregated nucleoli showed the highest capacity for retaining uranyl ions. This selective staining of the nucleolar (possibly proteinic) material proved also efficient in cells from Drosophila testes and Allium roots.

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Observations on the selective demonstration of nucleolar material by protein staining techniques in epon thick sections.

The effect of different protein stainings on thick sections of Epon embedded salivary glands of Chironomus pallidivittatus is described. Pretreatment of sections with several metallic salts affected the affinity for aniline blue black in different structures. The uranyl and aluminium ions followed by aniline blue black resulted in a highly selective nucleolar staining which proved also efficient in Allium cepa meristematic cells and which seems useful for the preferential demonstration of nucleolar material in thick sections.

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