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E. E. SWIERSTRA

Summary.

Four methods of measuring daily sperm production (DSP) were evaluated using seventy-two boars. The DSP was determined; I, by unilaterally castrating boars 0 and 48 hr after depletion of the epididymal sperm reserves and then measuring changes in the reserves (fourteen boars) ; II, by measuring changes in the epididymal sperm reserves of four groups of boars killed 5, 24, 52 and 72 hr following depletion of the reserves (forty-six boars) ; III, by dividing the total number of spermatozoa in the right and left epididymis of sexually active boars by the epididymal transit time (twelve boars) ; IV, by quantitative testicular histology (same twelve boars as for Method III). Method I was unsuitable for estimating the DSP of individual boars because of normal variation in sperm numbers between epididymides within boars. Method II revealed that there was too much variation in epididymal sperm reserves among boars to obtain a reliable mean estimate of DSP for the forty-six boars. Method III did not give reliable results for individual boars because epididymal transit time varies among boars. It was concluded that the DSP of individual boars could best be measured by Method IV though Methods III and IV gave similar estimates for the mean DSP of the twelve boars (15·0 × 109 versus 16·2 × 109). The sperm output of these boars averaged 15×5 × 109/day when ejaculates were collected at 72-hr intervals, suggesting little or no absorption of spermatozoa from the epididymides or excretion of spermatozoa in the urine of sexually active boars. The mean DSP/g of net testis was 24·5 × 106 (S.E.±0·3) as determined by quantitative histology. Only spermatozoa from the cauda epididymidis were ejaculated during depletion.

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E. E. SWIERSTRA

Summary.

A procedure is described for measuring daily spermatozoa production (DSP) from quantitative testicular histology. The mean DSP, as determined by this procedure, was 16·5 × 109 for ten Yorkshire boars (av. age 11·2 months) and 17·8× 109for ten Lacombe boars (av. age 11·3 months). The spermatozoa output was 88% of the DSP for the Yorkshire boars and 83% of the DSP for the Lacombe boars when semen samples were collected at 48-hr intervals. Spermatozoa output was significantly correlated ( ±0·54) with spermatozoa production. The two breeds did not differ significantly with respect to DSP, but within breeds certain boars produced more spermatozoa than others (P<0·05). The DSP per gram of testis was 25·1 × 106 for Yorkshire boars and 24·3 × 106 for Lacombe boars (P>0·05). The relative volume of the testes occupied by spermatids with round nuclei did not differ significantly between breeds, among boars within breeds nor between right and left testes. This suggests that for the boar, spermatozoa production is mainly a function of testis size. Results obtained by the procedure for measuring DSP were not significantly influenced by different staining techniques.

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E. E. SWIERSTRA and R. H. FOOTE

Summary.

The cycle of the seminiferous epithelium of the rabbit was divided into eight stages, using as criteria the shape of the spermatid nucleus, the location of the spermatids and spermatozoa in regard to the basement membrane, the presence of meiotic figures and the release of spermatozoa from the lumen. The relative duration (frequency) of Stages 1 to 8 were 27·7, 13·4, 7·3, 11·0, 4·1, 15·7, 12·2 and 8·6%, respectively. Each stem cell (Type A spermatogonium) divided to produce two Type A spermatogonia. One of these was the starting cell for the next generation, while the other gave rise to two intermediate-type spermatogonia. Three more spermatogonial divisions followed, producing sixteen primary spermatocytes from one Type A spermatogonium, as is characteristic for the bull and the ram, but unlike the rat, mouse and hamster. It was estimated that only 3·1 spermatids were generated from one primary spermatocyte, suggesting that in the rabbit there is considerable degeneration of spermatogenic cells during the two maturation divisions.

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E. E. SWIERSTRA, M. R. GEBAUER, and B. W. PICKETT

Summary.

The cycle of the seminiferous epithelium of the stallion was divided into eight stages, using as criteria the presence of meiotic divisions, shape of the spermatid nuclei and location of spermatids with elongated nuclei in the tubule. The mean frequencies of stages 1 to 8 were 16·9, 14·9, 3·2, 15·8, 7·4, 13·5, 12·6 and 15·7%, respectively. The duration of one cycle of the seminiferous epithelium was 12·2 days (S.E.±0·1) as determined by injecting a single dose of 700 μCi of [3H]thymidine into each spermatic artery of six stallions and removing testes at different intervals after the isotope injection. The life-span of primary spermatocytes was 19·0 days, secondary spermatocytes 0·7 days, spermatids with round nuclei 8·7 days, and spermatids with elongated nuclei 10·1 days. Radioactive spermatozoa were observed in the caput epididymidis 35 days after [3H]thymidine injection. The volumetric percentages of testicular components were: spermatogonial nuclei, 0·6; primary spermatocyte nuclei, 4·2; secondary spermatocyte nuclei, 0·1; round spermatid nuclei, 2·1; elongated spermatid nuclei, 1·0; Sertoli cell nuclei, 1·6; tubular cytoplasm, 45·7; lumina, 3·4; basement membranes, 2·6; and intertubular spaces, 38·7%. The seminiferous tubules made up 61·3% of the testicular volume. The diameters of the seminiferous tubules varied significantly among stallions, but not among stages. The average length of the seminiferous tubules per testis was 2419 m (range 1667 to 3726 m).

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E. E. SWIERSTRA, J. W. WHITEFIELD, and R. H. FOOTE

Summary.

Quantitative and qualitative analysis of the seminiferous epithelium of rabbits treated with Amphotericin B (Fungizone) revealed that ten intravenous injections of Fungizone, at a dose level of 2·0 mg Fungizone/kg body weight/day, had no effect on the duration of the stages of the cycle of the seminiferous epithelium, but affected the spermatozoa prior to their release from the seminiferous tubules. Fungizone decreased the rate at which the spermatozoa migrated from the Sertoli cells towards the lumen. Thus, spermatozoa which normally are released prior to Stage 1 were retained in some Stage 1 tubules of injected animals. A single local injection of Fungizone, at a dose level of 0·2 mg/ kg, into the cava vaginalis did not result in any observable change of the seminiferous epithelium. Unilateral castration had no effect on spermatogenesis in the remaining testis.