Seasonal Changes In Spermatogenesis Research Articles

Spermatogenesis in the giant anteater (Myrmecophaga tridactyla)

The giant anteater (superorder Xenarthra) is listed as Vulnerable by the International Union for Conservation of Nature (IUCN) and a low reproductive rate is considered one of the factors contributing to population decline of the species. Nevertheless, little is known on reproductive features in male giant anteaters and, in this regard, microscopic testis morphology and spermatogenesis were studied in roadkill specimens in Brazil. Characteristics of germ cell populations resembled descriptions in other eutherian mammals including other xenarthran species. Furthermore, eight stages of the seminiferous epithelium cycle could be defined. The proposed staging system offers baseline data for assessing impairments or seasonal changes in spermatogenesis and thus allows future studies on reproductive health and reproductive seasonality in male giant anteaters.

Testicular morphology and spermatogenesis in harbour porpoises (Phocoena phocoena)

Knowledge about reproductive parameters in male harbour porpoises such as testicular histology and germ cell maturation as well as seasonal changes in spermatogenesis is scarce. Thus, the aim of the present study was to report changes in the histological appearance of the testicular morphology of neonatal and juvenile harbour porpoises during maturation, to identify stages of spermatogenesis in adult males and to detect seasonal modifications. The identification of these stages can be used to assess the developmental profile of gene expression during spermatogenesis and to identify defects in spermatogenesis arising in pathological conditions. Testes of adult male harbour porpoises from the North and Baltic Sea that became stranded or by-caught in the years 1998–2016 were histologically examined using Haematoxylin and Eosin – staining. The Periodic Acid Schiff (PAS) staining was used for spermatogenic staging and the evaluation of the development of the acrosomic cap. For the identification of changes in testes morphology and morphometry during the course of the year, histological characteristics like germ cell associations and diameter of the convoluted seminiferous tubules were noted for each month. The analysis showed that in adult males more than one stage of spermatogenesis could be found per cross section of the convoluted seminiferous tubules similar to findings in men and some ape species. This rare phenomenon is called multi-stage-arrangement. In sexually active males from the peak breeding season (June and July) eight stages of spermatogenesis were identified and all stages occurred simultaneously, while during the low breeding season (August to May) only residual spermatogenesis or constituent germ cell populations were found. Missing germ cell generations were recorded in specimens from July to September. Our investigations provide a detailed staging of spermatogenesis and give new insight into the reproductive biology of male harbour porpoises. With these new basic parameters, indicators for endocrine disruptors can be developed in the future, aiming to detect how environmental factors could affect male fertility in wildlife.

Seasonal expression of androgen receptor, aromatase, and estrogen receptor alpha and beta in the testis of the wild ground squirrel (Citellus dauricus Brandt).

The aim of this study was to investigate the seasonal expression of androgen receptor (AR), estrogen receptors α and β (ERα and ERβ) and aromatase cytochrome P450 (P450arom) mRNA and protein by real-time PCR and immunohistochemistry in the wild ground squirrel (WGS) testes. Histologically, all types of spermatogenic cells including mature spermatozoa were identified in the breeding season (April), while spermatogonia and primary spermatocytes were observed in the nonbreeding season (June), and spermatogonia, primary spermatocytes and secondary spermatocytes were found in pre-hibernation (September). AR was present in Leydig cells, peritubular myoid cells and Sertoli cells in the breeding season and pre-hibernation with more intense staining in the breeding season, whereas AR was only found in Leydig cells in the nonbreeding season; P450arom was expressed in Leydig cells, Sertoli cells and germ cells during the breeding season, whereas P450arom was found in Leydig cells and Sertoli cells during pre-hibernation, but P450arom was not present in the nonbreeding season; Stronger immunohistochemical signal for ERα was present in Sertoli cells and Leydig cells during the breeding season; ERβ was only expressed in Leydig cells of the breeding season. Consistent with the immunohistochemical results, the mean mRNA level of AR, P450arom, ERα and ERβ were higher in the testes of the breeding season when compared to pre-hibernation and the nonbreeding season. These results suggested that the seasonal changes in spermatogenesis and testicular recrudescence and regression process in WGSs might be correlated with expression levels of AR, P450arom and ERs, and that estrogen and androgen may play an important autocrine/paracrine role to regulate seasonal testicular function.

The germ cell development strategy and seasonal changes in spermatogenesis and Leydig cell morphologies of the spiny lizard Sceloporus mucronatus (Squamata: Phrynosomatidae)

The viviparous lizards of the Sceloporus genus exhibit both seasonal and continuous spermatogenesis. The viviparous lizard Sceloporus mucronatus from Tecocomulco, Hidalgo, Mexico, exhibits seasonal spermatogenesis. This study demonstrates the relationship between changes in testis volume, spermatogenesis activity, and Leydig cells during the male reproductive cycle of S. mucronatus. A recrudescence period is evident, which starts in the winter when testicular volume is reduced and climaxes in February, when the greatest mitotic activity of spermatogonia occurs. The testicular volume and Leydig cell index increase gradually during the spring with primary spermatocytes being the most abundant cell type observed within the germinal epithelium. In the summer, the secondary spermatocytes and undifferentiated round spermatids are the most abundant germinal cells. The breeding season coincides with spermiogenesis and spermiation; testicular volume also increases significantly as does the Leydig cell index where these cells increase in both cytoplasmic and nuclear volume. During fall, testicular regression begins with a significant decrease in testicular volume and germinal epithelium height, although there are remnant spermatozoa left within the lumen of the seminiferous tubules. During this time, the Leydig cell index is also reduced, and there is a decrease in cellular and nuclear volumes within these interstitial cells. Finally, during quiescence in late fall, there is reduced testicular volume smaller than during regression, and only spermatogonia and Sertoli cells are present within the seminiferous tubules. Leydig cells exhibit a low index number, their cellular and nuclear volumes are reduced, and there is a depletion in lipid inclusion cytoplasmically.

Seasonal Changes in Spermatogenesis and Peripheral Testosterone Concentration in Raccoons (<i>Procyon lotor</i>) in Hokkaido

Feral raccoons (Procyon lotor) have been increasing in number since 1979 and are currently subject to pest control in Hokkaido. One of the reasons for the increase in numbers is thought to be the high reproductive potential of raccoons, but little is known about their reproduction. The main aim of this study was to clarify seasonal changes in spermatogenesis and peripheral testosterone concentration of raccoons in Hokkaido. In the present study, external characteristics and histology of the testis and epididymis and the plasma testosterone concentration were investigated in 68 feral, male raccoons culled for pest control and once a month in one live, captive male. The feral males exhibited seasonal changes in spermatogenesis, showing active spermatogenesis in autumn, winter and spring (October-June) with noted spermatogenesis and inactive spermatogenesis in summer (July-September) with lower mean levels of spermatozoa in the cauda epididymis. Even in the inactive period, spermatozoa were observed in about half of the individuals (14/26); therefore, individuals producing spermatozoa existed every month throughout the year. Testosterone concentrations were significantly high in the winter mating season. In the captive male, the testosterone concentrations were low from June to August, and spermatozoa could not be observed from July to September. These results suggest that raccoons exhibit seasonality of reproduction, but the time and duration of spermatogenetic decline varies widely among individuals. This individual variation in the inactive period is a feature of male raccoon reproduction and is unique among seasonally breeding mammals.

Seasonal Changes in Spermatogenesis and Immunolocalization of Cytochrome P450 17.ALPHA.-Hydroxylase/c17-20 Lyase and Cytochrome P450 Aromatase in the Wild Male Ground Squirrel (Citellus dauricus Brandt)

The purpose of this study was to investigate seasonal changes of spermatogenesis and the cellular localization of P450c17 and P450arom in wild male ground squirrels during the breeding and non-breeding seasons. The testicular weight, testicular size and score count of spermatogenesis from April to September were measured, and histological and immunohistochemical observations of testicular tissues were performed in wild male ground squirrels. In addition, total proteins were extracted from testicular tissue in the breeding and non-breeding seasons and were used for Western blotting analysis for P450c17 and P450arom. There were marked variations in testicular weight, testicular size and score count of spermatogenesis from the breeding season (April) to the non-breeding season (September). Histologically, spermatogonia, primary spermatocytes, secondary spermatocytes and spermatozoa were identified in the breeding season (April). Immunolocalization of P450c17 was detected in Leydig cells and spermatozoa during the breeding season and was only found in Leydig cells during the non-breeding season. The positive signals of P450c17 by Western blotting were both observed in the breeding and non-breeding seasons. Immunolocalization of P450arom was observed in Leydig cells, Sertoli cells and all types of spermatogenic cells including mature-phase spermatozoa in the breeding season, while immunoreactivity for P450arom was not present in the testis of the non-breeding season. With P450arom antibody, a band was also only detected in the breeding season by Western blotting. These results suggest that the seasonal changes in testicular weight and size are correlated with spermatogenesis and immunolocalization of P450c17 and P450arom, and androgen and estrogen may play an important role in the spermatogenesis and testicular recrudescence and regression process.

Seasonal Changes in Spermatogenesis and Immunolocalization of Inhibin/Activin Subunits in the Wild Male Ground Squirrel (<i>Citellus dauricus Brandt</i>)

The objective of this study was to investigate the seasonal changes in spermatogenesis and the immunolocalization of the inhibin alpha and inhibin/activin (betaA and betaB) subunits during the breeding and non-breeding seasons in the wild male ground squirrel. The testicular weight and size and seminiferous tubule diameter were measured, and histological observations of testes were performed. The sections of the testes were immunostained by the avidin-biotin-peroxidase complex method (ABC) using polyclonal antisera raised against porcine inhibin alpha, inhibin/activin betaA and inhibin/activin betaB during the breeding and non-breeding seasons. There were marked variations in testicular weight and size and seminiferous tubule diameter between the breeding and non-breeding seasons, and all types of spermatogenic cells, including spermatozoa, were found in the breeding season. In addition, immunoreactivity was also detected for the inhibin alpha, betaA and betaB subunits in Sertoli and Leydig cells during the breeding season, but immunostaining was only present for the inhibin alpha and inhibin/activin betaB subunits in Sertoli cells during the non-breeding season. These results suggest that seasonal changes in testicular weight and size and seminiferous tubule diameter of wild ground squirrels are correlated with changes in spermatogenesis, and the cellular localization of the inhibin/activin subunits showed season related changes in the breeding and non-breeding seasons.

Seasonally activated spermatogenesis is correlated with increased testicular production of testosterone and epidermal growth factor in mink ( Mustela vison)

Seasonal changes in spermatogenesis were studied with respect to testicular production of both testosterone and epidermal growth factor (EGF) in mink. The testes were collected in November ( n = 15; testis recrudescence), February ( n = 15; before breeding season), March ( n = 14; breeding season), and May ( n = 11; testis involution) and the following parameters of testicular activity were quantified: testicular mass, number of testicular spermatozoa, percentages of haploid, diploid, and tetraploid (G2/M-phase) cells and content of testosterone and EGF. The growth factor was immunohistochemically localized in the parenchyma. Testis mass, spermatogenic activity, and the production of both testosterone and EGF were maximal in March, but were not significantly different from the levels in February. The correlation between testis weight and sperm per testis was r = 0.825 ( P < 0.001). Testosterone and EGF levels were correlated to each other ( r = 0.78; P < 0.001) and had significant positive correlations to testis mass, number of sperm and proportion of haploid cells; and negative correlations to percentages of mitotic cells. EGF was localized in interstitial cells and in the luminal region of seminiferous tubules, where it occurred during the last steps of spermiogenesis. We inferred that intensified seasonal spermatogenesis was stimulated by testosterone and by autocrine/paracrine effects of EGF.

Seasonal differences in spermatogenesis, testicular mass and serum testosterone concentrations in the grizzly bear

Abstract The objectives of this study were to determine whether there are seasonal changes in spermatogenesis for pre-pubertal and post-pubertal grizzly bears (Ursus arctos horribilis), and investigate the seasonal association between testis mass and serum testosterone (T) concentrations for post-pubertal grizzly bears from the continental US from May through October. Testes from 25 grizzly bears were collected from bears killed by federal and state wildlife personnel in Montana and Wyoming from 1978 to 1995. Fifty blood samples were obtained from wild, post-pubertal (≥5.5 years) male grizzly bears from May through October in Montana and Wyoming from 1993 through 1995. In pre-pubertal bears, the seminiferous tubules were small and surrounded by abundant interstitial tissue in May. Tubules were enlarged and closely packed July through September. Tubules began to degenerate in November. Although spermatogonia and spermatocytes were present from May through September, spermatids never occurred within seminif...

Seasonal changes in spermatogenesis and testicular steroidogenesis in wild male raccoon dogs (Nyctereutes procynoides).

Testes of 15 wild adult male raccoon dogs (Nyctereutes procynoides) obtained from September 2000 to April 2001 were studied to clarify seasonal changes in spermatogenesis and testicular steroidogenesis. There were marked seasonal variations in the testis weight and size with values relatively low in September and highest in March. Spermatogonia and primary spermatocytes were observed in September, while spermatogonia, spermatocytes and round spermatids were present in January, and all types of spermatogenic cells including mature spermatozoa were found in the mating season (February and March). The number of spermatogenic cells reached their peak values in February and March. In addition, steroidogenic enzymes were immunolocalized using polyclonal antisera raised against bovine adrenal cholesterol side-chain cleavage cytochrome P450 (P450scc), human placental 3beta-hydroxysteroid dehydrogenase (3 betaHSD), porcine testicular 17alpha-hydroxylase cytochrome P450 (P450c17), and human placental aromatase cytochrome P450 (P450arom). P450scc and P450c17 were identified in Leydig cells and spermatids in February, whereas these enzymes were present only in Leydig cells in September. 3betaHSD was found in Leydig cells in September and February with more intense staining in February. The localization of P450arom changed seasonally: no immunostaining in September; more extensive immunostaining in Leydig cells, Sertoli cells, and elongating spermatids in February. These results suggest that seasonal changes in the testis weight and size of wild male raccoon dogs are correlated with changes in spermatogenesis. Seasonal changes in testicular steroidogenesis suggest that the synthesis of androgen and estrogen reaches its peak in the mating season.

Spermatogenesis, serum testosterone levels and immunolocalization of steroidogenic enzymes in the wild male Japanese black bear (Ursus thibetanus japonicus).

Twenty-one wild male Japanese black bears (Ursus thibetanus japonicus) were captured in the summer-autumn of 1998-2000 in the vicinity of Neo Village, Gifu Prefecture. Testes were measured, and testicular samples were biopsied and observed histologically. Four steroidogenic enzymes, i.e., cholesterol side-chain cleavage cytochrome P450 (P450scc), 3beta-hydroxysteroid dehydrogenase (3betaHSD), 17-alpha hydroxylase cytochrome P450 (P450c17), and aromatase cytochrome P450 (P450arom) were immunolocalized. Serum testosterone concentrations were measured by radioimmunoassay. Testis size changed little from 1-3 years of age, increased rapidly at 4 years, and attained its peak at 5 years. Serum testosterone concentrations ranged from 0.05 to 1.78 ng/m l, and the mean +/- standard deviation was 0.43 +/- 0.48 ng/ml. Age of sexual maturation in wild male Japanese black bears was estimated to be 3-4 years. Seasonal changes in spermatogenesis were obvious; active in June, July and August, degenerated by September. Leydig cells, Sertoli cells and germ cells have the capability of synthesizing androgen, and Leydig cells, Sertoli cells, spermatids and spermatogonia have the capability of synthesizing estrogen in Japanese black bears.

Relationship between seasonal changes in spermatogenesis in the juvenile ostrich (Stuthio camelus) and the presence of the LH receptor and 3beta-hydroxysteroid dehydrogenase

The immunohistochemical localization of the LH receptor and 3beta-hydroxysteroid dehydrogenase (3beta-HSD) was studied in the testis of the juvenile ostrich (Stuthio camelus) throughout a 1 year period. Spermatogenic activity of juvenile birds changed throughout the year, as has been reported previously for sexually mature birds. During the active stage of the testicular cycle, from September to January, spermatogenesis progressed up to the stage of formation of spermatozoa, although spermatozoa could not be detected in the epididymis. Leydig cells stained intensely with antibodies against the LH receptor and 3beta-HSD during the quiescent, recrudescent and active phases of the testicular cycle. During the regressive phase, there was a slight decrease in immunostaining for 3beta-HSD in these cells. These results indicate that Leydig cells in the testis of the juvenile ostrich are able to respond to LH and are capable of steroid synthesis. Furthermore, in juvenile (prepubertal) ostriches, spermatogeneic activity can be observed and, as in mature birds, spermatogenesis undergoes seasonal changes.

Relationship between seasonal changes in spermatogenesis in the juvenile ostrich (Stuthio camelus) and the presence of the LH receptor and 3beta-hydroxysteroid dehydrogenase

Relationship between seasonal changes in spermatogenesis in the juvenile ostrich (Stuthio camelus) and the presence of the LH receptor and 3beta-hydroxysteroid dehydrogenase

Seasonal changes in spermatogenesis of the Japanese lesser horseshoe bat, Rhinolophus cornutus from a morphological viewpoint.

Seasonal changes in spermatogenesis of Japanese lesser horseshoe bats, Rhinolophus cornutus, captured in Aomori Prefecture (Japan) were examined by light microscopy. In March, the seminiferous tubules revealed almost no lumen. The seminiferous epithelium consisted of Sertoli cells and spermatogonia. The interstitium occupied a relatively large area. In June, the seminiferous tubules gradually increased in diameter. Lumen was clearly seen at the center of seminiferous tubules. Mitotic figures of spermatogonia and spermatocytes were occasionally recognized. Interstitium occupation was still abundant. In August, the diameter of seminiferous tubules maximized. The interstitium occupied only a small area. Active spermatogenesis was obvious at this time. Released spermatozoa were frequently observed within the expanded lumen. In October, although spermatogenesis was still active, the diameter of seminiferous tubules tended to decrease in size. In December, active spermatogenesis completely disappeared. The diameter of tubules greatly decreased. In most cases, the seminiferous epithelium contained only Sertoli cells and spermatogonia. Thus, spermatogenesis in Japanese lesser horseshoe bats occurs from the middle or late summer to the middle autumn in Aomori Prefecture. In epididymal tracts, aggregated spermatozoa were recognized throughout the year. The cytoplasm of all Leydig cells in the interstitium was positive for 3beta-hydroxysteroid dehydrogenase throughout the year.

Seasonal changes in spermatogenesis and testicular steroidogenesis in the male black bear Ursus americanus.

American black bears, Ursus americanus, are seasonal breeders with a mating season in late spring to early summer. The objectives of this study were to determine whether there are seasonal changes in spermatogenesis and immunolocalization of testicular steroidogenic enzymes, and to correlate these changes with peripheral steroid concentrations. Three captive mature bears were maintained in open cages during the summer season and provided with chambers for denning during the winter. Testicular biopsies and blood samples were obtained from anaesthetized bears on 12 March, 15 June, 12 October and 15 January. Steroidogenic enzymes were immunolocalized using polyclonal antisera raised against bovine adrenal cholesterol side-chain cleavage cytochrome P450 (P450scc), human placental 3 beta-hydroxysteroid dehydrogenase (3 beta HSD), porcine testicular 17 alpha-hydroxylase cytochrome P450 (P450c17) and human placental aromatase cytochrome P450 (P450arom). Spermatogenesis changed seasonally: spermatogonia and degenerating spermatocytes were observed in October; spermatogonia and primary spermatocytes were present in January; spermatogonia, spermatocytes and round spermatids were present in March; and spermatogonia through spermatozoa were present in June. P450scc and P450c17 were immunolocalized in spermatids and Leydig cells in June, whereas in October these enzymes were present only in Leydig cells. 3 beta HSD was localized in Leydig cells in June and October with more intense staining in June. Localization of P450arom changed seasonally: no immunostaining in October; positive immunostaining in Sertoli cells in January; more extensive immunostaining in Sertoli cells, peritubular-myoid cells and round spermatids in March; and strong immunostaining in Sertoli cells and round and elongating spermatids in June. Serum testosterone and oestradiol concentrations changed seasonally: testosterone and oestrogen were low in October and January, slightly higher in March, and high in June. The present study demonstrates that in the black bear seasonal changes in spermatogenesis are accompanied by changes in the immunolocalization of testicular steroidogenic enzymes that are correlated with changes in serum testosterone and oestradiol concentrations. The presence of P450arom in Sertoli cells at the beginning of testicular recrudescence suggests that aromatase and oestrogen may play a role in re-initiating spermatogenesis.

Seasonal Changes in Spermatogenesis and Ultrastructure of Developing Spermatids in the Japanese Rat Snake, Elaphe climacophora.

Seasonal changes in spermatogenesis and the ultrastructure of developing spermatids in the Japanese rat snake, Elaphe climacophora, were observed by light and transmission electron microscopy. Spermatogenesis in this species began in August, continued through October and ceased in November. No spermatozoa were found during other periods. Japanese rat snakes mate from May to July, and spermatogenesis occurs after the mating season. Therefore, according to Girons' classification (1982), the reproduction of this species was classified as a postnuptial type. Although the morphological changes in developing spermatids during spermiogenesis in these snakes fundamentally resembled those in mammals, some unique features were detected. The most prominent characteristic of the developing spermatids was lipid-like structures. These structures first appeared in early round spermatids, gradually increased in size and number, and, finally, aligned around the nucleus of mature spermatids. Although spermatozoa with lipid-like structures were released from the epithelium, stored spermatozoa in vas deferenses had none of these structures. Lipid-like structures that apparently separated from spermatozoa were scattered in the vas deferens. Prominent elongation of mitochondria was also remarkable in elongated spermatids.

Seasonal Changes in Spermatogenesis (Including Germ Cell Degeneration) and Plasma Testosterone Concentration in the Grey-headed Fruit Bat, Pteropus poliocephalus

Maximal testicular size of P. poliocephalus occurred during the February-March-April period (autumn breeding season) associated with maximal plasma levels of testosterone (121' 5 � 23� 4 nmol/I). Testicular size decreased after the breeding season concomitant with a decrease in plasma testosterone (7'6 � 1�7 nmol/I). Histologically, regressive changes were observed in the testis after the breeding season including a decrease in seminiferous tubule diameter and a decrease in Leydig cell nuclear diameter. Significant germ cell loss occurred during the breeding season (44%) mainly during the final spermatogonial division and meiosis and increased in regressed testes (69%), being accentuated chiefly at meiosis. All regressed testes showed some sperm production although it was much reduced after the breeding season; however, optimal fertility appears to be restricted to autumn by the large increases in testosterone secretion which only occur at this time.

Seasonal changes in spermatogenesis in the blue fox (Alopex lagopus), quantified by DNA flow cytometry and measurement of soluble Mn2+ -dependent adenylate cyclase activity.

The testes of the blue fox (Alopex lagopus) showed marked seasonal variations in size. Testicular weight and volume increased rapidly during January and February to reach maximal values by the beginning of the breeding season (approximately 15 March). During May and June the weights and volumes of the testes declined gradually to the quiescent state which lasted from July until October. Quantitation by DNA flow cytometry of the seasonal changes in the relative numbers of haploid (1C), diploid (2C) and tetraploid (4C) cell numbers in the testis showed that the increase in testis size from December to February was associated with a rapid expansion of the haploid cell compartment as spermatogenesis resumed. In addition, an increase in number of more mature cell types within the haploid cell population was observed over a 2-month period before the breeding season. The decline in testicular size from the middle of April until October was associated with a reduction in both the absolute and relative sizes of the haploid and tetraploid cell populations and a concomitant increase in the relative numbers of diploid cells. Measurements of the activity of the soluble Mn2+ -dependent adenylate cyclase revealed seasonal variations that closely paralleled those of the haploid cell population, indicating that, as in other species, the enzyme may be associated with maturing germ cells.

Duration of spermatogenesis in the vole (Microtus agrestis) and bank vole (Clethrionomys glareolus).

Department of Agricultural Science, University of Oxford, U.K. The duration of the cycle of the seminiferous epithelium is a fundamental parameter of spermatogenesis in mammals (Heller & Clermont, 1964). Its measurement in the field vole (Microtus agrestis) could clarify the way in which seasonal changes in spermatogenesis in this species (Clarke & Forsyth, 1964) are brought about. Furthermore, in our laboratory colonies puberty in M. agrestis occurs at about 6 weeks of age, whereas in the bank vole (Clethrionomys glareolus) it is 5-6 weeks later (Greig, 1968). The duration of the seminiferous epithelial cycle has therefore also been estimated in C. glareolus to determine whether this dissimilarity is associated with a difference in the duration of the cycle of the seminiferous epithelium. As in other species (Roosen-Runge, 1962), spermatogenesis in M. agrestis (Grocock, 1972; Grocock & Clarke, 1975) and C. glareolus (Grocock, 1972) can be divided into 8 stages whose

Seasonal changes in spermatogenesis in rams : Their relation to plane of nutrition and to vitamin A status

Observations have been made on the seminal characters, body weights, and plasma vitamin A status of rams fed on carotene-deficient diets, at higher and lower levels of food intake. Carotene supplements were provided for a number of the rams at each level of dietary intake. The seminal characters exhibited a seasonal variation, characterized by a reduction in the total number and longevity of spermatozoa during the summer months. Within this period, a temporary increase in the number of morphologically abnormal spermatozoa occurred in the rams of low plasma vitamin A status, or on the lower plane of nutrition. Plasma vitamin A levels fell more rapidly in the rams on the higher plane of nutrition than in those on the lower plane. Morphological abnormality of spermatozoa attributed to vitamin A deficiency appeared at an earlier date in the high-plane group except when rams with presumably low liver stores of vitamin A were fed on the deficient diets. Vitamin A deficiency, if sufficiently severe, resulted in the appearance of a high percentage of morphologically abnormal spermatozoa in the semen of rams on both planes of nutrition. The addition of pure carotene to the diet prevented or reduced this degree of abnormality.