A Biometrical Study of the Influence of Size of Brood Cell Upon the Size and Variability of the Honeybee (Apis mellifera L.)
by Roy A. Grout, 1931
 









EXPERIMENTAL

After weighing, each bee was placed in a numbered vial containing tap water at room temperature and throughout the following treatment was recognized as a definite individual. After being in the water for 24 hours, the bees were soft enough for dissection. With the aid of a Spencer Binocular Microscope, containing a 3.5x ocular and a 55 mm. objective, and an ordinary dissecting set, the right fore wing, the third tergite, the fourth tergite and the proboscis of each bee were dissected. The dissected parts were then mounted directly upon numbered glass slides with Bueston's medium* and cover glasses were applied.

*Bueston's Medium for Mounting
Water ...................... 50 c.c.
Glycerine .................. 20 c.c.
Gum Arabic ............... 40 gm.
Chloral Hydrate ......... 50 gm.
Dissolve Gum Arabic in water. When dissolved, add Chloral Hydrate. When this is dissolved, add Glycerine. Filter.


All linear measurements were taken by a projection method. The numbered glass slide was placed in a Leitz Simple Micro-Projector in a vertical position and projected upon a movable screen attached to the opposite wall. Upon the face of the screen was a horizontal and vertical scale and the screen was so constructed that the entire face could be rotated around its center in a plane perpendicular to the line of projection. This feature greatly facilitated measuring the projected parts since the measuring scale could be turned to any desired angle at which the part to be measured might happen to lie. The projection measurement apparatus was arranged so that a glass Spencer stage micrometer, having a scale 2 mm. in length ruled to 0.01 mm., placed in the Micro-Projector gave a corresponding projection of 2 mm. magnified 127 times on the scale of the movable screen.

The apparatus was calibrated by this method before and at intervals during each long series of measurements. It was thus possible to read directly the exact measurement of the part in hundredths of a millimeter. However, for the sake of convenience and in order to eliminate any personal equation involved in the reading of actual measurements of the parts of the bee, a reading was taken at the beginning of the part and another at its end, the true measurement being the difference between the two readings. Plate 1 diagrammatically shows the measurements taken on the right fore wing, the third tergite and the fourth tergite. Following the system used by Michailov (43), the widths of the third and fourth tergites were combined and the summation of the two widths was used thruout the computation.

Plate 1.
Diagram showing measurements of right fore wing and tergites 3 and 4.


Plate 2 diagrammatically shows the measurements of the proboscis. In this manner the length of the submentum, the length of the mentum and the length of the glossa were obtained, the summation of the three lengths being the length of the proboscis. In only one group of bees was the length of the second member of the labial palpi taken.

Plate 2.
Diagram showing measurements taken of the proboscis.
G = from tip of labellum to anterior part of mentum.
M = length of mentum.
S-M = length of submentum.
L = length of 2nd member of labial palpi.
Length of proboscis = G + M + S-M.


The computation of the statistics was accomplished by recording the values of the measurements of each individual bee on a Hollerith Electric Tabulating and Accounting Machine. From the summations obtained in this manner, the arithmetic means, standard deviations, correlation coefficients, regression equations and other statistical constants were computed with the aid of a Monroe Calculating Machine. All formulas and methods used in the above computations are given by Wallace and Snedecor (69) in their bulletin entitled "Correlation and Machine Calculation" as revised by Snedecor in 1931.
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