Seasonal anatomical variations in the testes of European pike, Esox lucius L.

The seasonal development of the testes in European pike was examined using wild fish and biopsies from pike housed in tanks. The size of the tubules and the different cell types were measured and their histological appearance described. Four stages of development can be distinguished during the annual cycle. They are: (I) the stage of rest from June to August; (II) the stage of development from September to November with intensive spermatogenesis; (III) the stage of maturity from December to March/April with spermatogenesis completed; and (IV) the post-spawning stage from March to May.     

Effect of an LHRH agonist on pituitary and testicular function in rhesus monkeys

Male rhesus monkeys were given 100 micrograms [(imBzl)-D-His6,Pro9-NEt]-LHRH (LHRH-A), a potent LHRH agonist, s.c. daily for 40 weeks. The first dose of LHRH-A caused acute increases (2-4 h after injection) in serum LH (50-fold), FSH (2 X 5-fold) and testosterone (15-fold) concentrations. Chronic treatment led to a 95% decrease in LH and FSH responses. In spite of a marked decrease in LH response the effect on testosterone response was less evident. Administration of 50 i.u. hCG to control and LHRH-A-treated animals showed that the testicular steroidogenic response was unimpaired by the chronic treatment. Evaluation of the electroejaculated semen at regular intervals showed that there was no consistent reduction in the sperm count of LHRH-A-treated monkeys. Testicular biopsies showed that normal spermatogenesis was occurring in all treated animals, but testicular volume was significantly decreased. These results suggest that, in rhesus monkeys, the pituitary is more susceptible to desensitization by chronic LHRH agonist treatment than are the testes, and that LHRH agonists do not have direct antitesticular effect in rhesus monkeys.     

Effect of continuous infusion of a low dose of GnRH antagonist on serum LH and testosterone concentrations, spermatogenesis and semen quality in the rhesus monkey (Macaca mulatta)

Treatment of 4 adult male rhesus monkeys for 8-12 months with 100-400 micrograms of a GnRH antagonist/day by means of using osmotic minipumps led to suppressed serum concentrations of LH and testosterone followed by various degrees of recovery toward pretreatment values. The serum LH response to a challenge of native GnRH was reduced by 30-75% during antagonist treatment. The serum testosterone response to GnRH was exaggerated above the response in the pretreatment period, suggesting hypersensitivity of the testis to gonadotrophin. Antagonist administration under these conditions did not alter body weight or abolish ejaculatory response. Antagonist infusion caused a 96% decrease in sperm counts. Spermatozoa recovered during the final month of antagonist treatment showed a reduced ability to penetrate denuded hamster ova. Testicular biopsies performed at the end of antagonist treatment revealed persistent spermatogenesis. However, the cellularity of the seminiferous tubules was decreased below that of pretreatment biopsies. The results of this study suggest that the amount of testosterone needed to maintain normal spermatogenesis is greater than that needed to maintain electroejaculatory response in monkeys.     

The seasonal pattern of testosterone secretion in finn cross rams in Israel

Three adult Finn cross rams were bled at 30-min intervals for 7 h in March, May–June, August and November, and again at hourly intervals for 2 h after an intravenous injection of 50 μg of a GnRH analogue. Plasma testosterone concentrations were measured by radioimmunoassay. The mean testosterone level from 15 blood samples for each ram was highest in November and lowest in March. The episodic pulse pattern of testosterone secretion during the 7-h blood sampling periods was most evident, and more similar among rams in August and November, and less so in March and May.The mean testosterone concentration from the blood samples collected 1 and 2 h after GnRH injection was significantly higher in August–November than in March–June, but the ratio of the testosterone level after to that before injection was highest in March and lowest in November.     

Seasonal differences in plasma testosterone profiles in buffalo bulls

Testosterone was measured by radioimmunoassay in blood samples collected hourly over 10 h from two adult buffalo bulls in April, May, August and December. The basal concentrations were below 0.2 ng/ml while peak concentrations ranged from 0.35 to 1.65 ng/ml, with not more than one complete peak occurring during a 10 h period. Both bulls had similar testosterone profiles within each sampling period but differences were evident between periods, the mean concentration being highest in August and falling through December and April to the lowest levels in May. Testosterone concentrations in buffaloes are therefore lower than those in other domestic species, and appear to vary during different times of the year.     

Seminal parameters in rhesus monkeys under physiological conditions and in studies for male fertility control using FSH antibodies or LH-RH-agonists

To characterize the male rhesus monkey as a nonhuman primate model for human testicular functions, parameters of exocrine and endocrine testicular function were monitored in 16 adult male-rhesus monkeys for 1 and 5 years respectively. Testicular volumes in-season (October–January) were twice as great as in out-of-season animals (March–June). Ejaculations, both spontaneous and electrostimulated, ceased out-of-season. In 37 ejaculates obtained by electrostimulation in-season, sperm counts ranged from 110–1,100 million/ejaculate, 65% of sperm were motile and 60% were normally formed. Testicular histology showed regression of spermatogenesis out-of-season, with the diameter of the tubules being only one third of that in-season. Circannual changes in exocrine testicular function were accompanied by parallel fluctuations in pituitary and endocrine testicular functions, as evidenced by basal hormone levels and the production rate of testosterone, as well as the response to LH-RH throughout the year. As FSH is required for spermatogenesis in rhesus monkeys, we initiated a study on the long-term effects of active immunization against FSH as a possible means of fertility control. After the first 2 years of observation we can conclude that the production of specific antibodies to FSH results in suppression of spermatogenesis (oligospermia and occasional azoospermia) without affecting endocrine function. The lack of adverse side effects may encourage further investigations on this approach to fertility control. LH-RH-agonists exert degenerative effects on testicular function in rats via a down regulation of the pituitary and testis. A 12 week treatment of four adult monkeys in-season with Hoe 766 (Hoechst; 4μg/day for eight weeks, 20μg/day for 4 weeks sc) did not reveal any change in sperm counts or motility, although some pituitary desensitization was evident. It remains to be investigated whether even higher doses may result in a suppression of spermatogenesis.     

Influence of photoperiod on the seasonal pattern of secretion of luteinizing hormone and testosterone and on the antler cycle in roe deer (Capreolus capreolus).

Annual variations in concentrations of luteinizing hormone (LH) and testosterone in plasma were analysed in relation to the antler cycle in six adult male roe deer exposed to a natural photoperiod (latitude 46 degrees 10'N) and in four adult males maintained in a constant short-day photoperiod (8 h light: 16 h dark) for a year, from the winter solstice at which time both groups of animals had antlers in velvet. The animals were sampled, every 15 min for 2 or 4 h at intervals of one month for a year. Under both natural and experimental conditions, LH concentrations were high from January to March, but in the experimental conditions they decreased between April and May-June, whereas in the natural conditions they increased. Plasma LH concentration was lowest between July and November in animals under natural photoperiod, whereas under 8 h light:16 h dark photoperiod a second increase in plasma LH occurred between August and September. Between March and August, concentrations of plasma testosterone increased under natural photoperiod, whereas under experimental photoperiod there was a biphasic pattern of plasma testosterone with peaks between February and May and between September and November. Under natural photoperiod, antlers were cast in November, 369 +/- 6 days after the previous antlers were cast. Under experimental photoperiod, antlers were cast after 193 +/- 10 days, and a new set developed. The sexual cycle of the male appears to be initiated by an endogenous rhythm in winter and is then maintained by hormonal changes resulting from increasing photoperiod in spring.(ABSTRACT TRUNCATED AT 250 WORDS)     

Pituitary-gonadal hormones during prolonged residency in Antarctica

 Plasma luteinizing hormone (LH), follicle stimulating hormone (FSH), prolactin (PRL) and testosterone levels were measured in nine eugonadal men in New Delhi and during the 1st week of different months of their stay at Dakshin Gangotri in Antarctica. During their 12-month stay in Antarctica, they were exposed to a severely cold climate, long polar nights and polar days, high wind velocity, increased amounts of solar and ultraviolet radiation and geomagnetism, as well as physical and social isolation. Plasma testosterone tended to increase in March, but a significant increase (P<0.05) was not seen until April. The mean testosterone levels in May, June, September and November were also significantly higher than the March or New Delhi values. The absolute values of LH, FSH and PRL did not show any month-to-month changes in Antarctica. However, when the hormone levels were expressed as a percentage of the individual annual Antarctic mean, significant differences as a percentage of the individual annual Antarctic mean, significant differences were observed. The testosterone peak in April, May and June was associated with an increase in LH. The nadirs of testosterone, LH, FSH and PRL were seen in either July or August. FSH showed the highest values in March, whereas the highest PRL values were seen in November. These observations suggest the presence of circannual variations in gonadotropin, PRL and LH in Antarctica which are independent of polar days and polar nights. It appears that factors other than the duration of daylight might be involved in regulating these changes. The significance of maintenance of testosterone levels in the supra-physiological range in Antarctica remains unknown but may be important in acclimatization/habituation to the extreme polar cold by increasing basal metabolic rate, protein synthesis and erythropoiesis. Received: 13 October 1997 / Accepted: 13 February 1998     

Reproductive characteristics and gamete development of the soft coral Sclerophytum cf. heterospiculatum in Okinawa Island,Japan

Sexual reproduction data are important to understand how organisms can replenish their populations and proliferate on coral reefs. Despite the importance of such data, the reproductive characteristics of most soft coral species are still unknown. Here, we examined the reproductive strategies of a species from the often-dominant genus Sclerophytum in a coral reef on subtropical Okinawa Island, Japan. DNA barcoding and histological examinations of the tissues were conducted to confirm colony conspecificity and identify reproductive characteristics, respectively, between March 2020 and March 2021. Results indicated that the studied species, identified as Sclerophytum cf. heterospiculatum, exhibits gonochorism with longer oogenesis and shorter spermatogenesis. Female colonies produced immature oocytes throughout the year, with mature oocytes observed from late July to early September, and thus, extended spawning is likely characteristic of this species. In male colonies, spermatogenesis took place over ~5 months, with spermaries present from April through August. Mature spermaries were noted beginning in July and the inferred peak of sperm release was between late August and early September, which suggests that spermatogenesis duration was ~5 months. The largest mean oocyte and spermary sizes (628.45 ± 61.36 and 240.04 ± 49.49 μm, respectively) were both recorded in August. Gamete spawning presumably occurred during the summer season, which suggests seasonality in reproduction as influenced by changes in seawater temperature. However, the proximate cue for exact dates of spawning could be the lunar period because the inferred release of spawning materials seemed to occur between full moon and last-quarter moon phases in both the months of August and September. The results of this study represent the first detailed report of reproductive characteristics of the genus Sclerophytum in Japan.     

The development of seasonal variation in gonadal hormones and body weight in the maturing squirrel monkey

Captive-born squirrel monkeys of three different subtypes (Colombian, Bolivian, Peruvian), ranging in age from 1 to 4.5 years for males and 1 to 3.5 years for females, were examined at 3-month intervals throughout the year for seasonal changes in levels of plasma testosterone and progesterone and in body weight. Cyclical activity of testosterone in males began between 2 and 3 years of age but became more defined by the time the animals were 3–4 years old. Peak values occurred in February and May and corresponded to the the time of year in which adults normally mate. Elevations of progesterone occurred initially at approximately 2.5 years of age in February and May, and mainly infernales of the Colombian subtype. However,unlike levels of testosterone in males of this age, which declined in August and November (following the typical breeding season), levels of progesterone in females continued to increase during these months. Seasonal changes in body weight were also found in males but these changes were less evident than, and did not correlate with, hormonal changes.     

The reproductive cycle of the Nile crocodile (Crocodylus nilotkus)

The reproductive cycle of the Nile crocodile ( Crocodylus niloticus ) was studied in Zimbabwe. Females attained sexual maturity after they had reached a total length of about 262 to 287 cm and males, 270 to 295 cm. Some adult females did not reproduce every year. Follicle growth and vitellogenesis occurred from April to mid August during the dry winter. During this time reproductive females had elevated levels of plasma oestradiol-17β, testosterone, calcium and magnesium, but lowered levels of iron. The measuring of plasma calcium was an 'early pregnancy' test, reliable up to four months before nesting. Elevated levels of plasma testosterone in reproductive females corresponded to the time of courtship and mating. Ovulation occurred during the latter half of August. Males had viable sperm from mid May to mid September, during the winter. Courtship and mating occurred from late June to mid August, when crocodiles were confined to pools. Females nested on the higher sand ridges in the dry river bed from early September to early October, and eggs hatched during December.     

Reproductive Cycle of the American Alligator

The reproductive cycle of the American alligator, Alligatormississippiensis, was studied using blood and tissue samplesfrom wild alligators, and blood samples drawn from a captivebreeding stock at the Rockefeller Wildlife Refuge in Louisiana.Generally the cycle commences in March as air and water temperaturesincrease. By early April the seminiferous tubules are full ofactively dividing spermatocytes and maturing spermatids. Testismass is greatest at this time and plasma testosterone is ata peak (>50 ng/ml), but mature spermatozoa do not appearuntil late April and mid May when mating takes place. Plasmatestosterone levels decline rapidly in June after spermiation,and are low to nondetectable in July and August when the testesare fully regressed. A second small peak in testosterone occursin September without any obvious changes in testicular histology.In the female a similar temperature dependent initiation ofthe ovarian cycle occurs in late March. Plasma estradiol levelsreach a peak (>600 pg/ml) in mid April, and ovarian folliclesincrease from 5 mm to 45 mm in diameter at ovulation in May.Plasma testosterone is also high in preovulatory females (ca.1.5 ng/ml). Plasma progesterone shows a periovulatory surgeto levels as high as 16 ng/ml, but declines rapidly during the3 wk between ovulation and oviposition. During egg incubation(66 days) when the female remains close to the nest, ovariansteroids remain undetectable.     

Age-related changes in diurnal rhythms and levels of gonadotropins, testosterone, and inhibin B in male rhesus monkeys (Macaca mulatta)

Testosterone shows circadian rhythms in monkeys with low serum levels in the morning hours. The decline relies on a diminished frequency of LH pulses. Inhibin B shows no diurnal patterns. In elderly men, the diurnal rhythm of testosterone is blunted and inhibin levels fall. Here we explore whether aging exerts similar effects in the rhesus monkey. We collected blood samples from groups of young (6-9 yr) and old (12-16 yr) male rhesus monkeys at 20-min intervals for a period of 24 h under remote sampling via a venous catheter. We determined moment-to-moment changes in plasma levels of testosterone, FSH, and LH by RIA, and of inhibin B by ELISA. We found significant diurnal patterns of testosterone in both groups. The circadian rhythm in testosterone was enhanced in older monkeys. Testosterone levels and pulse frequencies dropped significantly below those of young monkeys during midday hours. Diminished pulse frequency of LH appeared to be responsible for the midday testosterone decrease in old monkeys, while LH and testosterone pulse frequency did not change in young monkeys at corresponding time points. Old monkeys showed extended periods of LH-pulse quiescence in the morning and midday hours. Inhibin B and FSH levels were generally lower in old monkeys compared with the young group, but neither inhibin B nor FSH showed circadian rhythms. We conclude from these data that old rhesus monkeys have a more prominent circadian rhythm of LH and testosterone resulting from an extended midday period of quiescence in the hypothalamus-pituitary-gonadal axis.     

Longitudinal studies on annual changes in plasma testosterone,body weight and spermatogenesis in adult Japanese mankeys (Macaca fuscata fuscata) under laboratory conditions

The present study was undertaken to clarify the annual changes in testicular function of Japanese monkeys under laboratory conditions. Five adult males were kept in an air-conditioned room with artificial 12/12 hr lighting. Measurements of body weight and blood sampling were conducted monthly for 13 months. The concentrations of plasma testosterone were determined by radio-immunoassay. The testicular size was measured and testicular tissues taken by biopsy were examined histologically at the four seasons. The body weight and plasma testosterone levels showed coincidental annual changes with a peak in September and a nadir in March or May. The percentage of seminiferous tubules including pachytene spermatocytes and the number of pachytene spermatocytes in tubular cross-sections were significantly increased in both the autumn and winter and decreased in the spring. Electron microscopically, the seasonal change was reflected in an increased size of fat granules in Sertoli cells in the breeding season.     

Seasonal changes in plasma testosterone concentrations and Leydig cell and accessory gland activity in the Cape horseshoe bat (Rhinolophus capensis)

Male Cape horseshoe bats were studied in the Cape Province of South Africa (33 degrees 17'S, 26 degrees 25'E) between January 1983 and June 1985. The reproductive cycle is characterized by reactivation of the seminiferous tubules in early summer (October) after a 4-month (June to September) period of winter inactivity. Spermiogenesis occurred between January and April, and spermatozoa were released to the epididymides in April and May. Spermiogenesis was associated with Leydig cell activity and increasing plasma testosterone concentrations. At this time components of the reproductive accessory glands became secretorily active or showed increasing secretory activity. During winter Leydig cells were secretorily inactive and plasma testosterone concentrations dropped, but components of the accessory complex remained active. There was a second period of Leydig cell secretory activity and increasing and peak plasma testosterone values in late winter/early summer which may be associated with copulation or the initiation of a new cycle of spermatogenesis.     

Sex differences in plasma corticosterone in desert tortoises, Gopherus agassizii, during the reproductive cycle

Blood samples from 30 female and 20 male adult desert tortoises, Gopherus agassizii, were collected at monthly intervals during the annual reproductive cycle (April to October). Plasma corticosterone and the sex steroids in each of the samples were analyzed by radioimmunoassay. Mean corticosterone levels in males were significantly higher than in females (P < 0.001) in every month. Male tortoises showed a marked seasonal pattern in plasma corticosterone with a highly significant peak in July, August, September, and October that corresponded with a similar peak in plasma testosterone. Testosterone and corticosterone in the male showed a highly significant correlation (P < 0.0001). The pattern of corticosterone in the female was less marked, with a significant peak in May during the mating and nesting season, but no association with the peak in estradiol in late summer was apparent. The highest levels of corticosterone in the males were associated with the peak in spermatogenesis and intense male-male combat. These results support similar data from other reptiles that suggest increased glucocorticoid secretion during periods of increased activity and metabolism.     

A study of seasonally delayed puberty in the male hare, Lepus Europaeus.

The brown hare, Lepus europaeus, has a mating season which extends from January to September. Adult males exhibit pronounced seasonal changes in the reproductive tract which are associated with changes in LH secretion. Maximum plasma levels of immunoreactive LH occur between March and June and minimal levels in the autumn non-mating period from September to December; this seasonal cycle in gonadotrophin output is reflected by the appropriate changes in the secretion of testosterone from the testes and in the activity of the accessory sex glands. Juvenile animals reach puberty only during the adult mating season, and the age of puberty thus varies with the date of birth. Males born before May reach puberty and become fertile at 3 months of age, while those born from May to July grow to a mature body size during the autumn non-mating season but puberty is delayed for several months. Since some animals experiencing delayed puberty were found to have elevated plasma levels of LH and testosterone, it is concluded that puberty is not completely suppresed by the environmental effects of the autumn, but that the developmental process is prolonged, resulting in the juveniles being synchronized with the adults in their reproductive activity.     

The influence of breed,season and photoperiod on semen characteristics,testicular size,libido and plasma hormone concentrations in rams

Twenty-seven adult rams (9 Suffolk, 9 Texel and 9 Dorset Horn) were raised under natural photoperiod and were trained to serve into an artificial vagina. On 1 April they were abruptly exposed to 3 different photoperiods as follows: (i) 8 hours light and 16 hours darkness (8L : 16D); (ii) 16 hours light and 8 hours darkness (16L : 8D); (iii) natural photoperiod. All rams were kept at pasture daily between 09.30 h and 16.00 h except when required indoors for experimental work. Rams on artificial photoperiod had appropriate supplemental lighting in an environmental chamber. Semen collection was attempted from each ram on alternate weeks during the experiment which lasted for 6 months. Semen was evaluated for volume, density, motility and abnormalities. Testicular length and circumference were recorded at 2-week intervals and libido was recorded at 4-week intervals. Three blood samples were collected from each ram at 30-min intervals on a weekly basis and the plasma was stored at ?20°C until assayed for testosterone and prolactin.Photoperiod had no significant effect on semen volume, motility and percentage dead or abnormal cells. Breed of ram had a significant effect on semen motility (P < 0.05) with Dorset Horn rams producing semen with the highest motility. Volume and motility scores both increased as the breeding season approached (P < 0.05), while the percentage of abnormal cells decreased (P < 0.01). Breed or photoperiod did not significantly affect scrotal measurements although animals exposed to 8L : 16D had the highest measurements. Month affected testicular measurements which generally increased from April to September. Suffolk rams had higher testosterone concentrations, and this breed also completed the highest number of mounts within an allocated test time (P < 0.05). Dorset Horn rams reached a peak in testosterone concentrations in June/ July whereas Suffolks and Texels reached a similar peak in August. Prolactin concentrations decreased from a maximum at the start and rams on natural photoperiod tended to have highest levels. These results show that month can have a bigger influence on semen characteristics than imposed artificial photoperiods in rams which have been exposed to increasing natural daylength for some months.     

Variation in plasma lipids during the reproductive cycle of male and female desert tortoises,Gopherus agassizii

Plasma triacylglycerol, phospholipid, cholesterol, cholesterol esters, fatty acids, and total lipids were measured in 30 female and 20 male desert tortoises (Gopherus agassizii) during the annual reproductive cycle in the eastern Mojave desert, Nevada. Blood samples were collected at monthly intervals from April to October. All lipid fractions, with the exception of free fatty acids, were significantly higher in female plasma than in male plasma in all months of the year. In contrast, free fatty acids were higher in male plasma than in female plasma in all months. The seasonal pattern in estradiol secretion mirrored that of triacylglycerol, phospholipid, cholesterol, and total lipid, all of which showed a significant correlation with the hormone. Estradiol and the vitellogenesis-associated lipids were all significantly higher in August, September, October, and April than in June. The seasonal variation in cholesterol ester levels in females did not correlate with any of the reproductive events and did not appear to be involved in yolk precursor formation. Total lipid in males showed a negative correlation with testosterone and spermatogenesis. Individual fatty acids in the June and August samples (at the highest and lowest estradiol levels) were compared in male and female plasma. The percent of C18:3n3, C18:2n6, C18:1n9, C20:5n3, and C22:5 were significantly higher in the June female plasma sample than in the August sample. Docosahexanoic (C22:6n3) acid was barely detectable in female plasma in either month.     

The seasonality of births in Canada

Earlier studies on the seasonality of births indicate that a major peak occurs in August and September and a minor peak in January and February. This study uses the 1984 Canadian Fertility Survey data on reproductive history to examine birth and pregnancy seasonalities, and shows that the 'worst' months for births are January and February and the 'best' months are March, April and May. There is no systematic pattern in the seasonality of pregnancies, possibly because effective birth control allows couples to plan the timing of births.