Influence of Temperature upon the Time (in Minutes) Required From Insemination to the First Cell Division
| Temperature | Arbacia | Strongylocentrotus purpuratus | ||||
|---|---|---|---|---|---|---|
| Loeb and Wasteneys 1911 | Loeb and Chamberlain 1915 | |||||
| °C. | Minutes | Minutes | Minutes | |||
| 3 | 532 | |||||
| 4 | 469 | |||||
| 5 | 352 | |||||
| 6 | 275 | |||||
| 7 | 498 | 291 | ||||
| 8 | 410 | 411 | 210 | |||
| 9 | 308 | 297 | .5 | 159 | ||
| 10 | 217 | 208 | 143 | |||
| 11 | 175 | 175 | ||||
| 12 | 147 | 148 | 131 | |||
| 13 | 129 | |||||
| 14 | 116 | 121 | ||||
| 15 | 100 | 100 | 100 | |||
| 16 | 85 | .5 | ||||
| 17 | 70 | .5 | ||||
| 18 | 68 | 68 | 187 | |||
| 19 | 65 | 178 | ||||
| 20 | 56 | 56 | 175 | |||
| 21 | 53 | .3 | 178 | |||
| 22 | 47 | 46 | 175 | |||
| 23 | 45 | .5 | Upper temperature limit | |||
| 24 | 42 | |||||
| 25 | 40 | 39 | .5 | |||
| 26 | 33 | .5 | ||||
| 27 | .5 | 34 | ||||
| 30 | 33 | |||||
| 31 | 37 | |||||
These figures permitted the determination of the temperature coefficients Q10 with a sufficient degree of accuracy (see next table). It seemed of importance to attempt to decide what the chemical reaction underlying these reaction velocities is (if it is a chemical reaction). Loeb and Wasteneys[255] investigated the temperature coefficient for the rate of oxidations in the newly fertilized egg of Arbacia and found that the temperature coefficient Q10 for that process does not vary in the same way as the temperature coefficient for cell division.
TABLE XI
Temperature Coefficients Q10 for the Rate of Segmentation and Oxidations in the Eggs of Strongylocentrotus AND Arbacia
| Temperature | Q10 for Rate of Segmentation in | Q10 for Rate of Oxidations in Arbacia | ||
|---|---|---|---|---|
| Strongylocentrotus | Arbacia | |||
| °C. | ||||
| 3– | 13 | 3.91 | 2.18 | |
| 4– | 14 | 3.88 | ||
| 5– | 15 | 3.52 | 2.16 | |
| 7– | 17 | 3.27 | 7.3 | 2.00 |
| 8– | 18 | 6.0 | ||
| 9– | 19 | 2.04 | 4.7 | |
| 10– | 20 | 1.90 | 3.8 | 2.17 |
| 11– | 21 | 3.3 | ||
| 12– | 22 | 1.74 | 3.1 | |
| 13– | 23 | 2.8 | 2.45 | |
| 15– | 25 | 2.5 | 2.24 | |
| 16– | 26 | 2.6 | ||
| 17.5– | 27.5 | 2.2 | 2.00 | |
| 20– | 30 | 1.7 | 1.96 | |
It is obvious that the temperature coefficient of the rate of oxidations is remarkably constant, about 2 for 10°, for various temperatures and does not show the variation from 7 or more to 2.2 for Q10 for the rate of segmentation.
Kanitz[256] has shown that in a graph in which the logarithms of the segmentation velocities are drawn as ordinates and the temperatures as abscissæ the logarithms form two straight lines which are joined at an angle. According to the law of van’t Hoff and Arrhenius concerning the influence of temperature upon velocities of chemical reactions the logarithms should lie in a straight line. We are dealing therefore in these cases with two exponential curves, one representing in Arbacia the interval 7–13° and the second from 13–26°; in Strongylocentrotus between 3–9° and 9–20°.
It was found in these experiments that if measurements of the Q10 of later stages of development are attempted the variations due to unavoidable difficulties become too great to permit an equal degree of reliability in the determinations.
The vast importance of this influence of temperature upon the rate of development is seen in the fact that in addition to the food supply the rate of the maturing of plants and animals depends on this factor.