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combination to evaluate an ejaculate. As indicated previously, the combined use of<br />

computerized semen analysis systems and zona-free hamster ova penetration assays may<br />

prove to be a powerful set of tools but the costs are currently prohibitive for most<br />

commercial production facilities. The following is a list of the more common ejaculate<br />

characteristics used for evaluation.<br />

1. Concentration (millions of sperm/ml)<br />

2. Progressive motility (%)<br />

3. Acrosome morphology (% intact acrosomes)<br />

4. Volume (ml)<br />

5. Tail morphology (% abnormal)<br />

6. Mass motility (%)<br />

7. Ejaculate color<br />

8 pH<br />

Why do we bother to perform these evaluations? Even though fertility cannot be<br />

accurately predicted, the lack of it can. Deviations from the norm is usually a good<br />

predictor of low fertility. Our objective in evaluating semen quality should be to identify<br />

those samples that have traits pointing to the probability of below normal fertility and<br />

therefore discard them. An extension of this thought is to discard those males that<br />

continuously produce poor quality semen.<br />

In general, semen quality can be divided into two categories: a) the number of sperm<br />

cells harvested and b) the viability of the collected sperm cells. Quantification of sperm<br />

cells can be readily determined with the proper equipment and training. It is simply the<br />

product of the ejaculate volume and the sperm concentration.<br />

27

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