The development of computer automated sperm morphometry analysis (ASMA
) allows for the objective analysis of sperm head dimensions. A number
of studies have been performed to optimize the efficiency of these sy
stems when analyzing spermatozoa from a Variety of species. in this st
udy, frozen semen from 10 fertile goat bucks was thawed and prepared o
n slides for morphometric analysis to evaluate technical variation and
to standardize ASMA procedures for goat spermatozoa. Methods of stain
ing, the number of spermatozoa necessary to sample and optimal microsc
opic magnification were assessed. Staining for 20 min in hematoxylin (
HEM) was found to be optimal. The most efficient method of analyzing g
oat sperm morphometry was to evaluate 100 sperm cells at x20 objective
magnification. Using these techniques, a sample could be analyzed in
approximately 2 min. The system properly recognized and digitized sper
matozoa 96% of the time with a target recognition error rate of less t
han 1%. The morphometric measurements of sperm heads for all 10 bucks
were the following: length =7.69 mu m, width=3.80 mu m, width/length r
atio=0.5, area=22.82 mu m and perimeter=20.15 mu m. The mean coefficie
nts of variation (CV) for all bucks ranged from 3.4% for length to 5.8
% for area. Standardized sample preparation techniques and analysis we
re found to improve the efficiency of ASMA.