The Kansas University Science Bulletin, Vol. I, No. 2, February, 1902Various
Science
The Kansas University Science Bulletin, Vol. I, No. 2, February, 1902
Various
Science -- Periodicals
Transcriber's Notes:
Underscores "_" before and after a word or phrase indicate _italics_
in the original text.
Small capitals have been converted to SOLID capitals.
Typographical errors have been silently corrected but other variations
in spelling and punctuation remain unaltered.
The quotations in German appear to have some errors, but these
quotations have been reproduced exactly as in the original paper.
THE KANSAS UNIVERSITY SCIENCE BULLETIN.
(VOL. I, NO. 2—FEBRUARY, 1902.
Whole Series, Vol. XI, No. 2.)
CONTENTS:
SPERMATID TRANSFORMATIONS IN GRYLLUS ASSIMILIS,
WITH SPECIAL REFERENCE TO THE NEBENKERN.
—_W. J. Baumgartner._
PUBLISHED BY THE UNIVERSITY,
LAWRENCE, KAN.
Price of this number, 30 cents.
Entered at the post-office in Lawrence as second-class matter.
KANSAS UNIVERSITY SCIENCE BULLETIN.
VOL. I, NO. 2. FEBRUARY, 1902. {WHOLE SERIES,
{VOL. XI, NO. 2.
SPERMATID TRANSFORMATIONS
In Gryllus assimilis, with Special Reference to the Nebenkern.
(Thesis for the degree of Master of Arts.)
BY W. J. BAUMGARTNER.
With Plates II and III.
I.—METHODS.
II.—MATERIAL.
III.—OBSERVATIONS.
(_a_) NUCLEUS.
(_b_) Cytoplasmic Structures.
1. Nebenkern.
2. Acrosome.
3. Axial Filament.
4. Centrosome.
5. Cell Body.
(_c_) The Spermatozoon.
IV.—COMPARISON OF RESULTS.
V.—SUMMARY.
It is the object of these studies to follow carefully the spermatid
transformations, and, if possible, to get a complete series of
changes occurring therein. I do not pretend that I have as yet found
all the stages, but in the present paper will publish observations
made on _Gryllus assimilis_ pertaining chiefly to the nebenkern, of
which I have found some stages not previously described, as far as I
know. I shall first describe my own findings, and then compare them
with the results of others.
I. Methods.
While other fixing agents were used, Flemming’s chromo-acetic-osmic
mixture (strong) proved the best. Its fixation was satisfactory in
all but a few stages, where the chemical changes going on in the cell
are such that it seems difficult, probably impossible, to secure
good, clear results; at least, neither Gilson’s nor Zenker’s mixture
did any better on cells in these stages.
Heidenhain’s iron-hæmatoxylin stain gave the best results, although
Flemming’s three-color method was very satisfactory.
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