Book - The development of the frog's egg (1897) 16

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Chapter XVI Effects of Temperature and of Light on Development

It has been long known that the rate of development within certain limits is dependent on temperature. The development of the frog's Qg^ is very much retarded, or even stopped, in water at the freezing-point. In North America, Rana temporaria often lays its eggs so early in the spring that the water is afterward frozen. The eggs that are caught in the ice are generally killed, but those that lie in the water below often remain alive and will subsequently develop normally.


Hertwig ('94) has shown that the maximum temperature for normal development of the eggs of Rana fusca is about 25 degrees C. Eggs develop very rapidly at this temperature, and in twenty-four hours have reached a stage of advancement corresponding to that at the end of the second day for the average temperature of 16 degrees. A temperature of 25 to 30 degrees C. long continued, or a temperature of 30 to 35 degrees for a short time, injures the eggs ; their development is arrested and many die. Eggs that have been partially injured by heat (after two or three hours at 30 degrees C. or after three to eight hours at 26 to 28 degrees C. and then brought into a normal temperature) continue to develop at a slower rate than eggs under normal conditions. The yolkhemisphere of the Qgg is first affected, so that the cleavagefurrows do not appear in it. The injured or dead half of the Q^g lies below, and the segmented portion above.


Hertwig obtained similar results by cooling the eggs. Soon after fertilization the eggs were placed in water at zero C. and kept there for twenty-four hours. During that time they did not segment, but when brought back to a higher (normal) temperature, the Qgg divided into two, four, etc., blastomeres; nevertheless, as subsequenf development showed, the egg had been injured. Many of these eggs developed in the same way as did those kept at a temperature of 25 degrees C, i.e. the segmentation of the yolk-hemisphere was retarded.


Schultze ('95) has also made some experiments on the eggs of Rana fusca in which the eggs were subjected to a temperature of zero C. Embryos in the following stages of development were used : stage A, when the dorsal lip of the blastopore had just appeared ; stage B, at the end of the "gastrula " period ; stage C, embryos with closed medullary folds. Three days after these had been placed in a chamber at zero C. they were examined and found in the same stage as when put into the cold. Some of the eggs were then removed, and continued to develop normally at a higher temperature. After fourteen days in the cold the remaining eggs were examined. The eggs were still in the same stage as when put into the cold chamber, but those of stage C had died. The others developed normally when brought into a liigher temperature.


Thus while Hertwig found that the eggs of Rana fusca were injured by only twenty-four hours at a temperature of zero C, Schultze saw that certaiii stages^ at least, were not affected by fourteen days at the same temperature. It is to be noted that Hertwig put the eggs into cold water soon after fertilization, while Schultze used later stages of development.


Not only is the rate of development of the frog-embryo affected by the temperature, but also by the kind of light in which it develops. Schnetzler in 1874 compared the development of Rana temporaria in white and in green light. The conditions of the two sets of embryos were nearly the same except as regards the kind of light. The embryos developed much faster in the white light, and the tadpoles underwent sooner their metamorphoses. Yung ('78) made a much more careful and elaborate series of experiments in which the eggs and embryos were subjected to a series of different lights. Instead of colored glass, which is seldom monochromatic, Yung used solutions of different sorts. The eggs were placed in a vessel containing about 5 litres of water ; this vessel was then placed in a larger vessel of the same form. A space of 5 to 10 mm. was left between the two vessels. This space was filled with a fluid that allows only certain parts of the spectrum to pass through. The top of the dish containing the eggs was covered by an opaque lid. An alcoholic solution of " fuchsine cerise " was used to produce a monochromatic red light ; a solution of potassium chromate for a yellow light (although this allows a little red and green to pass through) ; a solution of nitrate of nickel (which is perfectly monochromatic) for a green light; an alcoholic solution of aniline "bleu de Lyon" for a blue light ; and an alcoholic solution of aniline violet for a violet light. Parallel experiments took place in the daylight (" white light ") and in the dark. The other conditions were the same for all the aquaria ; they had the same amount of water, the same extent of surface for aeration, the same temperature^ and were placed in the same position before a window. Eggs of R. esculenta and of R. temporaria were used.


At the end of seven days it could be seen that the embryos in the violet and in the blue light were more vigorous and in a later stage of development than the others. At the same time the development in the red and in the green was retarded. At the end of a month the tadpoles were in good condition, and the following table shows their mean length in each aquarium.

Larvae of Rana Esculenta at the End of One Month.


Violet.


Blue.


Yellow.


White.


Dark.


Red.


Green,


27


24


22.8


23


19.6


19.1


15.1


The breadth of the embryos shows the same differences. It is interesting to see that in the red and in the green light the tadpoles were even less developed than those in the white light or even in the dark. The result of this series of experiments on R. esculenta agrees with other experiments made by Yung at different times, upon other species of frogs and upon other animals.


Appendix

METHODS OF PRESERVATION, ETC.

For general purposes the eggs and embryos may be preserved in a saturated solution of picric acid in seventy per cent, alcohol to which a little sulphuric acid has been added (as in Kleinenberg's picro-sulphuric solution). The segmenting eggs or the early stages of the embryo surrounded by the jelly should be put directly into the fluid. Each egg should have, however, the outer jelly-coats cut off with a pair of scissors, and it is well to use an abundance of the preserving solution. Older embryos may be shelled out in the preserving fluid with sharp needles. After from three to five hours the eggs or embryos are transferred to seventy per cent, alcohol, which is changed several times ; they should be kept for several days in eighty per cent, alcohol. In this alcohol (eighty per cent.) the inner egg-membrane slowly separates from the Qgg^ and can be easily removed, after which the Qgg is preserved permanently in eighty-five per cent, to ninety per cent, alcohol. Corrosive-acetic solution gives good results with older embryos. For the early stages of fertilization and of extrusion of the polar bodies the following solution is to be recommended : one per cent, chromic acid, twenty-five parts ; water, seventy parts ; glacial acetic acid, five parts. Boiling water also gives good results.

Difiiculty is often found in cutting the eggs on account of the brittleness of the yolk-portion ; but if the following method is carefully followed, there will be no trouble in this regard. The preserved Qgg or embryo is put into absolute alcohol from two to five hours, turpentine two to three hours, soft paraffine a half-hour (change once), hard paraffine a half-hour. The melting-point of the hard parafiine should be from 56 to 58 degrees C. The egg miist then be cut at a temperature of seventy-five to eighty degrees Fahrenheit (24 to 26 degrees C); one often succeeds best if the microtome is placed in the sunlight during the cutting.

The segmentation-stages do not need to be stained. The okler embryos stain well in toto in borax carmine or in hsematoxylin on the slide. Fresh material cuts and stains better than that long preserved.

Formalin preserves eggs and jelly most admirably for demonstration. The segmentation-stages show particularly well when preserved (permanently) in this solution.



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Pages where the terms "Historic" (textbooks, papers, people, recommendations) appear on this site, and sections within pages where this disclaimer appears, indicate that the content and scientific understanding are specific to the time of publication. This means that while some scientific descriptions are still accurate, the terminology and interpretation of the developmental mechanisms reflect the understanding at the time of original publication and those of the preceding periods, these terms, interpretations and recommendations may not reflect our current scientific understanding.     (More? Embryology History | Historic Embryology Papers)
Frog Development (1897): 1 Formation of the Sex-cells | 2 Polar Bodies and Fertilization | 3 Cross-fertilization Experiments | 4 Egg Cleavage | 5 Early Embryo | 6 Germ-layers | 7 Abnormal Embryos with Spina Bifida | 8 Pfluger's Experiments | 9 Born and Roux Experiments | 10 Cleavage Modification | 11 Effect of Blastomere Injury | 12 Interpretations of Experiments | 13 Endoderm | 14 Mesoderm | 15 Ectoderm | 16 Temperature and Light Effects | Literature | Figures

Morgan TH. The development of the frog's egg: an introduction to experimental embryology. (1897) The Macmillan Co. London.


Cite this page: Hill, M.A. (2020, August 10) Embryology Book - The development of the frog's egg (1897) 16. Retrieved from https://embryology.med.unsw.edu.au/embryology/index.php/Book_-_The_development_of_the_frog%27s_egg_(1897)_16

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