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Volume 58, 1928
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Analytical Data.

Although no attempt at complete analysis of these oysters was made, in order to make up diets correctly it was necessary to know the approximate percentage of fat and water. Some nitrogen estima-tions were also made. These data are presented here in Tables 1 and 2.

Table 1.
Date Average weight per oyster. Fat percentage Glycogen percentage Remarks.
Aug, 1924 10 grm. 2.58
June, 1925 7 grm. 1.90
Aug., 1925 ? 1.96
Oct. 12, 1925 10 grm. 2.6 non-spawning
Oct. 12, 1925 8 grm. 2.2 spawning
Oct. 31, 1925 9.5 grm. 2.44 4.1 non-spawning
Oct. 31, 1925 6.4 grm. 1.57 1.6 spawning
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It may be noted that the fat in these oysters was lower than that previously reported in 1911 and less than the estimation made in 1924. The glycogen and fat of the fourth batch of oysters was higher than the others, which may be due to the fact that they were from new ground. While these variations may be expected when the oysters are not dredged from one special area, and when no note of age is taken, one feature of the analysis is a striking one, viz., the difference between the “non-spawning,” and the “spawning” or “spawned.” This difference is seen in the average weight per oyster, the fat and the glycogen, while we have just shown that the spawned oyster has less vitamin-A.

A large proportion of the nitrogen of the oyster is present in non-protein form and this is probably the case in all shell fish for the

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Exp. 6. From A to B, equialent of more than 1 grm. fresh oyster (spawn-ing or spawned) given separately.—Compare to Exp. 5.
Exps. 7, 8. From A to B, equivalent of 1 grm. fresh oyster per rat daily. Ak. 2 (upper) received non-spawning oyster. Ak. 3 (lower) received spawning or spawned oyster.

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same result in nearly the same relative proportion was found in the paua as reported Paper 4 of this series. The method of distinguish-ing the two forms of nitrogen was as follows:—10 grm. fresh oyster had added to it 40 cc. water and the whole brought to boiling point. 150 cc. of 98 per cent. alcohol was then added and the mixture allowed to stand for a day at room temperature, then filtered, washed with alcohol, and nitrogen estimation made in both residue (protein) and filtrate plus washings (extractives).