Surface area and volume measurements were made for ram and human sperm
atozoa. Measurements were made using different techniques in an attemp
t to confirm estimates arrived at by independent methodologies. Sperm
head projected surface areas were calculated from published formulae u
sing linear micrometry measurements or were obtained directly by image
analysis. Total surface areas were calculated as twice the projected
head area plus the flagella area, estimated from published dimensions.
Spermatozoon surface area was also measured from electron micrographs
using a stereological method. Micrometric methods gave values of 135
mu m(2) for ram spermatozoa and 106 mu m(2) for human spermatozoa. Ste
reology methods gave values of 142 mu m(2) for ram spermatozoa and 106
.5 mu m(2) for human spermatozoa, offering good agreement between the
two methods. Sperm volumes were estimated by stereology and by radiola
bel volume exclusion methods. From stereology, ram sperm volume was 31
.3 mu m(3) and human sperm volume was 22.2 mu m(3). From the volume ex
clusion method, ram sperm volume was estimated as 25 mu m(3). Attempts
to measure total volume and water volume simultaneously using an adap
tation of this method were unsuccessful. Separate estimation of water
volume for ram spermatozoa gave a value of 12.8 mu m(3), suggesting a
50% water space. Results from this study are compared with existing pu
blished values.