As for the errors of erythrocytes counts, distribution of red corpuscles in the counting cell is of great importance. The author conducted examination of the depth of cell. Although cell-depth can be measured easily by microscope with microscrew, this method has not been used in practice, because of its inacuracy and the cell-depth is generally measured by some special apparatus. They are, however, very expensive and not accessible. The author improved the microscopic method for practical use. The improved points were as follows;
1) Particles of soot or pigment, and staphylococci were tried as the marks, which should adhere on the surface of ruled platform and coverglass. Staphylococci were quite suitable for this purpose, while soot and pigment were not because of their inaccurate foci.
2) As for the focus of staphylococcus-mark, in stead of real focus, a so-called F' point, which locates near real focus shall be selected, because the F' point can be adjusted more accurately than the others.
3) Owins to the inadequateness of gea-wheel, the reading of the F' point on microscrew by downward turning did not always agree with the reading by the reversed (upward) turning. Therefore, backward turning of microscrew should be absolutely avoided, until the reading of upper and lower marks were finished. Furthermore, turning of microscrew shold be started from the point locating 40 microscrew degrees higher than the upper mark.
4) The graduation of microscrew is not so accurate that the reading by it is more or less variable in accordance with the selection of starting point. Hence, it was required to settle a base point in order to minimize the error.
According to the above mentioned procedures, amount of error of measurement was examined. The findings were as follows: (at every observation, three successive measurements were made to obtain mean value, and the mean value is designated henceforth “observation value”)
a) Amount of variation of the observation value at each location of a counting cell, though a couple of marks at every observation was not always the same, did not exceed 0.6 micron.
b) Amount of variation of the depth of coating cell in consequence of the replacement of coverglass was negligibly small, if the coverglass was laid on the same side and from the same direction and the Newton's bands on the platform of both sides showed similar figures.
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