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The semen quality factor (SQF) takes into account 3 semen parameters as a means of predicting semen fertilizing ability: semen volume, semen concentration, and the percentage of live and morphologically normal spermatozoa. The objective of this study was to test the suitability of the SQF as an indicator of fertility for geese. Twenty-one ganders were divided into 3 groups based on their individual SQF values, and semen was pooled within each group. A fourth semen group was generated by diluting semen from the highest SQF group with 2 vol of diluent. Pooled semen was inseminated into 30 geese per treatment. Relationships between SQF and fertility were evaluated. Testosterone and estradiol levels in seminal plasma were determined by competitive immunoassays. The SQF values of the 4 diluted semen groups were 19.3, 11.3, 9.5, and 13.1, and the corresponding fertility values, determined by candling, were 83.9, 65.6, 56.8, and 74.3%, respectively. The correlation coefficient between SQF and fertility was 0.985 (P < 0.01), indicating that the SQF can be used as a good indicator of fertility for geese. The SQF values correlated well with the ratio of testosterone to estradiol in seminal plasma (r = 0.48, P < 0.05), which could also be a diagnostic tool for evaluating the reproductive potential of individual ganders.

Sex-linked dwarf chickens caused by the mutation of the growth hormone receptor gene are characterized by normal growth hormone (GH), very low insulin-like growth factor I (IGF-I) level in the blood, and reduced growth. It has been demonstrated that the sex-linked dwarfing gene has negative effects on female reproduction. In the current study, dwarf cocks and their phenotypic normal siblings were used to investigate the effects of dwarf gene on male reproduction. Dwarf cocks grew slower than the normal cocks did, and at 20 wk of age, their BW were 36.4% smaller. However, all parameters for semen quality, including volume, sperm concentration, viability, mobility, pH, and percentage of abnormal sperms, examined at 30 wk of age showed no significant difference between normal and dwarf cocks. The fertility of dwarf cocks was 95.2%, and the normal was 92.4%. The concentrations of GH and IGF-I in serum and seminal plasma were measured with RIA and ELISA, respectively. The serum GH in the dwarf cocks was significantly higher than their normal siblings (P < 0.05), whereas the serum IGF-I in the dwarf cocks was very low. However, the concentration of seminal IGF-I in dwarf cocks was similar to that of their normal siblings, indicating that IGF-I might be produced and acted independently in testis. In conclusion, the deficiency in GH receptor did not affect the male reproduction in dwarf chickens, and the fertility of dwarf cocks could be satisfactory for production when artificial insemination was adopted.