Ejaculation by male rhesus in the absence of female partners

The number of ejaculatory plugs found beneath the cages of male rhesus over a 14-month period indicated a high incidence of ejaculation in the home cage in the absence of a female partner. Frequency of ejaculation in the home cage was not related to concurrent tests of sexual behavior with receptive females. Moreover, ejaculation in the home cage within 22 hr or less of sex tests did not affect the frequency of ejaculation in tests with stimulus females. Long- and short-term vasectomized males ejaculated as frequently in their home cages as nonvasectomized males. No ejaculatory plugs, of course, were found beneath the cages of males castrated 2 years earlier.     

Copulatory behavior of male rats paired with natural proestrous and hormone-treated ovariectomized females

The male's sexual behavior paired with estrogen-progesterone primed induced ovariectomized receptive females was compared with natural proestrous females. The former showed longer ejaculation latency and more intromissions to the first ejaculation than the latter.     

Influence of androgen in the neonatal period on ejaculatory and postejaculatory behavior in the rat

The objective of the present report was to investigate the influence of androgen in the neonatal period on the development of ejaculatory and postejaculatory behavior. At birth, male rats were either castrated (neonatally castrated males), implanted with a Silastic tube of the aromatase inhibitor androsta-1,4,6-triene-3,17-dione for the first 10 days (ATD males), or left untreated (normal males). Female rats were either injected with 0.5 mg testosterone propionate (TP) on Days 1 (day of birth) and 2 (androgenized females) or left untreated (normal females). All gonadally intact animals were castrated at 60 days of age. Following TP administration, all animals were tested for ejaculatory and postejaculatory behavior under both shock and nonshock conditions. All animals were capable of showing the intromission pattern; however, the ejaculatory pattern was exhibited regularly only by those animals exposed to androgen at birth (normal males, androgenized females, and ATD males). The normal males required fewer intromissions to achieve ejaculation than the other two groups exhibiting this reflex. This result is discussed in terms of peripheral genital stimulation deficits and the differentiation of neural tissue responsible for masculine copulatory behavior. Androgenized females and ATD males displayed a refractory period, characterized by 22-kHz vocalizations, equal to or longer than that found in normal males. These results indicate that defeminization is not necessary for the display of normal ejaculatory and postejaculatory behavior.     

Influence of Female Copulation Calls on Male Sexual Behavior in Captive Macaca fascicularis

We investigated the function of copulation calls—vocalizations by females during mating—in captive groups of long-tailed macaques. We tested predictions of the contest-competition, sperm competition, synchronized orgasms, mate again, alpha-male notification and graded-signal hypotheses. We observed 371 copulations of 36 females wherein the presence or absence of a copulation call was clear. Females call equally often with different males and shortly after ejaculation. Copulation calls occurred equally with copulations with and without ejaculation. Calls did not incite disruptions of the mating. Following calls females mated again, more often than expected, with their mating partner. Both pregnant and fertile females uttered copulation calls. Two females conceived and mated mainly with the alpha male then. We conclude that copulation calls do not incite male contest competition for sexual access to females and that it is unlikely that calls synchronize male and female orgasms. Several hypotheses remain plausible, but not all predictions are borne out unequivocably. This alerts us to the possibility that the calls could have multiple beneficial effects; natural selection might strike a compromise among functions. Investigation of the mate again, sperm competition and alpha-male notification hypotheses, and of hypotheses not tested in our study concerning female breeding overlap and female-female agonism, is required.     

Ultrasonic Communication in Rats: Can Playback of 50-kHz Calls Induce Approach Behavior?

Rats emit distinct types of ultrasonic vocalizations, which differ depending on age, the subject's current state and environmental factors. Since it was shown that 50-kHz calls can serve as indices of the animal's positive subjective state, they have received increasing experimental attention, and have successfully been used to study neurobiological mechanisms of positive affect. However, it is likely that such calls do not only reflect a positive affective state, but that they also serve a communicative purpose. Actually, rats emit the highest rates of 50-kHz calls typically during social interactions, like reproductive behavior, juvenile play and tickling. Furthermore, it was recently shown that rats emit 50-kHz calls after separation from conspecifics. The aim of the present study was to test the communicative value of such 50-kHz calls. In a first experiment, conducted in juvenile rats situated singly on a radial maze apparatus, we showed that 50-kHz calls can induce behavioral activation and approach responses, which were selective to 50-kHz signals, since presentation of 22-kHz calls, considered to be aversive or threat signals, led to behavioral inhibition. In two other experiments, we used either natural 50-kHz calls, which had been previously recorded from other rats, or artificial sine wave stimuli, which were identical to these calls with respect to peak frequency, call length and temporal appearance. These signals were presented to either juvenile (Exp. 2) or adult (Exp. 3) male rats. Our data clearly show that 50-kHz signals can induce approach behavior, an effect, which was more pronounced in juvenile rats and which was not selective to natural calls, especially in adult rats. The recipient rats also emitted some 50-kHz calls in response to call presentation, but this effect was observed only in adult subjects. Together, our data show that 50-kHz calls can serve communicative purposes, namely as a social signal, which increases the likelihood of approach in the recipient conspecific.     

The length of the fertility period of the rat spermatozoa]

4-day cyclic Wistar female rats were caged with sexually experiences males at either 18:00-19:00 on proestrus or at 21:30-22:30 during the following night. 16 out of 17 bulbectomized females and 16 out of 40 intact females respectively mated at 18:00-1900. 22 out of 24 intact females mated at 21:30-22:30. Only 11 out of the 32 receptive females became pregnant in the first group while 14 out of the 22 receptive females went into pregnancy in the second group. It is then supposed, given that ovulation does not take place before midnight during the night from proestrus to estrus in the rat that the fertilizing capacity of spermatozoon is of relatively short duration in the rat.     

Female Iberian midwife toads (Alytes cisternasii) use call order to reach particular males in dense choruses

Call-timing mechanisms among anuran males calling within choruses are frequent, and previous studies have indicated that midwife toad females respond preferentially to these mechanisms. The results of multi-speaker tests performed here with midwife toads suggest that the temporal order of male calls within a dense chorus can determine the ability of females to locate the most attractive calls (in this instance the low-frequency calls emitted by larger males). When call emission was regular in the multi-speaker tests, most females chose the most attractive option (i.e., the speaker emitting the lower-frequency call). When call emission was not regular, however, most females failed to reach the most attractive option, selecting the speaker that emitted immediately after that emitting the most attractive call. These results support the idea that there may be benefits for smaller males that emit their less attractive calls close to those of larger, more attractive males in dense choruses. Less attractive males could exploit the attractiveness of nearby larger males calls by alternating their calls in an unordered sequence to reach receptive females.     

Copulatory behavior of sexually inexperienced male hamsters paired with natural proestrous females

The copulatory behavior of sexually inexperienced male hamsters paired with natural proestrous females was observed between 1900 and 2000 hours under dim red light illumination. Each male was allowed 30 min to mate with a receptive female. Five out of 7 males showed at least one ejaculation within 30 min. Although the copulatory behavior of the above males was observed again, the activities of copulatory behavior did not facilitate.     

Egg-oviduct interaction initiates reproductive behavior

The experiments reported in this paper provide evidence that eggs must pass through the oviducts in order for receptivity to occur after ovulation in the female frog, Rana pipiens. In one experiment, oviductectomized frogs remained unreceptive after ovulation was induced by administration of exogenous pituitary glands, while sham-operates became receptive within 48 hr. Another experiment had four groups of subjects: ovariectomized females, females with oviducts ligated at the ostial end, females with openings in the uteri that prevented eggs from accumulating there, and sham-operated females. Only the last two groups, groups in which eggs could pass through the oviducts, became receptive. In these experiments, receptivity was indicated by absence of the release call during manual clasping of the trunk. Earlier experiments have shown that eggs have to pass through the oviducts in order to become fertilizable. Thus, the passage of eggs through the oviducts provides a mechanism which links the onset of reproductive behavior to the availability of fertilizable gametes.     

Sexual motivation in the male rat: the role of primary incentives and copulatory experience.

Two experiments explored the motivational impact of primary incentive female cues on the operant behavior of sexually naive and experienced male rats. In the first experiment, a straight-arm runway was used to assess the subjects' motivation to approach a goalbox containing either male or female "targets." Twelve sexually naive Long-Evans males ran for: (1) an empty goalbox; (2) a male conspecific; (3) an ovariectomized (OVX) female; (4) an OVX female given estradiol; (5) or an OVX female treated with estradiol and progesterone. A perforated Plexiglas partition in the goalbox prevented the subject males from physically interacting with the targets, although olfactory, visual, and auditory cues were accessible. We hypothesized that subjects would manifest shorter run times (reflecting greater motivation) when the goalbox contained a receptive/proceptive female as opposed to a nonreceptive female target. Subjects' run times were ordered depending on the nature of the target (from slowest to fastest): empty goalbox, male conspecific, OVX female, OVX + estradiol female, and OVX + estradiol + progesterone female. As predicted, subjects ran significantly faster for a receptive/proceptive female than for a nonreceptive female, indicating that sexually naive males are inherently motivated by female precopulatory cues. In the second experiment, 30 sexually naive male subjects ran for a goalbox containing either a nonestrous (OVX) or an estrous (OVX + estradiol + progesterone) female. Following six trials, 10 males were allowed one intromission with a receptive female, 10 males experienced one ejaculation, and 10 remained sexually naive. Only those males having experienced an ejaculation subsequently decreased their run times for both nonestrous and estrous females, indicating that sexual reinforcement produced by ejaculation, but not intromission, further enhances the motivational impact of female incentive cues.     

Hormonal responses to different sexually related conditions in male rats

Plasma levels of corticosterone (C) and testosterone (T) increase after sexual activity in males of several species. However, the physiological significance of these increases has not been elucidated. In the present study, hormonal response to different conditions linked to sexual activity was assessed. In the first experiment, plasma levels of C and T were assessed both in sexually experienced and naive male rats after the following conditions: (A) control group, without sexual stimulation; (B) males exposed to ovariectomized females; (C) males exposed to intact, non-receptive females; (D) males exposed to receptive females with the vagina obstructed, to avoid intromission; (E) males exposed to receptive females: but separated by a grid that prevents physical contact; (F) males exposed to receptive females during 30 min. In a second experiment, experienced male rats were allowed to repeatedly copulate until reaching the criteria for sexual exhaustion, and 24 h later, they were allowed to copulate. Once sexually related conditions ended, males were killed and their blood was obtained. C and T plasma levels were assessed by HPLC with ultraviolet (UV) detection. Results indicate that T did not increase significantly in naive male in any sexual condition, while in the experienced males, significant increases were observed with the mere presence of a receptive female and also after ejaculation. These increases were significantly larger in experienced males. On the other hand, C also increased in all sexual conditions, both in experienced and naive rats; however, the increase observed was larger in experienced males. Regarding sexual satiety, both C and T increased after copulating ad libitum to satiety. T increased almost three-fold compared to control, while C increased two-fold. No significant changes were observed in either one of the steroids 24 h after sexual exhaustion, even though males remained with a receptive female during an hour. These results show that sexual experience has an important influence on the hormonal response to sexual activity. C rises could be directly related to sexual arousal involved in the different sexual conditions, while T rises seem to have a direct relationship with both the motivation and execution aspects of masculine sexual behavior.     

Ejaculations induced by p-chloroamphetamine (PCA) in rats, hamsters and mice.

The ejaculatory response induced by p-chloroamphetamine (PCA) in male rats, hamsters and mice was observed during 2 hours after the injection. The animals were treated intraperitoneally with PCA at doses ranging from 0.78125 to 160 mg/kg. The ED50 (effective dose in 50% of animals) values of PCA for the initiation of ejaculation in rats and hamsters were 1.3397 (1.0732-1.6725) and 0.1105 (0.0802-0.1522) mg/kg, respectively. On the other hand, no ejaculation was observed in any mice at any doses examined. So we concluded that there are species differences in the ejaculatory response, induced by PCA, among rats, hamsters and mice.     

Determinants of mating success in the golden hamster (Mesocricetus auratus): Social dominance and mating tactics under seminatural conditions

We tested the hypothesis that high social status leads to high levels of copulatory behaviour and increased number of offspring in hamsters. When paired with albino female golden hamsters, males of three genotypic strains showed differences in the frequency and temporal patterning of some measures of copulatory behaviour but did not differ in general fertilization success. The results of two-male, one-female tests in which mating order and ejaculation frequencies were controlled indicated only relatively small differences in differential fertilizing capacity among these genotypes. Males of the genotypic strains displayed an equal probability of achieving alpha status in three-male, one-female competitive mating tests in which animals were habituated to semi-natural enclosures. Alpha males often slept in the female's nest box the night before she became receptive, were the first to mate on the following morning, achieved higher scores for all measures of sexual behaviour including ejaculation frequency and subsequently sired more young than did lower ranking males. However, the differential reproductive success of alpha males was not simply a function of higher ejaculation scores since they obtained more than twice as many young per ejaculation as subordinate males. Alpha males continued to copulate with long intromissions after exhausting their supply of ejaculates. Although females mated with several males, mating preferences were evidenced by their flank-gland and vaginal marking patterns on the day before receptivity and in their initial choice of mates during tethered male tests. The behaviour of alpha males is consistent with previous findings regarding the effects of mating order and prolonged copulation on sperm competition and suggests that sperm utilization patterns and mating tactics have coevolved.     

Changes of heart rate during sexual behavior in the female rat.

The authors studied the physiological and behavioral responses during sexual behavior in female rats. For this purpose, electrocardiographs were recoded from conscious and unrestrained females using a radiotelemetry system. Heart rate during sexual behavior rose sharply following the introduction of a sexually active male, displayed a peak level of 425 bpm during male ejaculation, and then rapidly decreased. This pattern of heart rate in females before and after receiving ejaculation was similar to that in males before and after ejaculation. In the rate of decrease in heart rate, however, there was a significant difference between females and males. The present study is the first to show changes of heart rate during sexual behavior in female rats.     

Control of attractivity and receptivity in female red-sided garter snakes

Female red-sided garter snakes emerge from their hibernacula in the spring attractive and receptive to males. Attractivity is communicated by a pheromone released through the female's skin and is a consequence of ovarian recrudescence the previous summer. Receptivity, on the other hand, is stimulated by ovarian estrogen secretion during emergence itself. Mating renders females both unattractive and unreceptive. Another "mating" pheromone of male origin is important in making females unattractive after mating. To investigate the role of cloacal stimulation in the loss of attractivity and receptivity we injected a local anesthetic (lidocaine or tetracaine) in the cloacal region of females before mating. This does not prevent mating, although it blocks neural transmission of copulatory sensory stimuli. The time course of transition from attractive and receptive states was then observed. Females treated with local anesthetic as well as control females were unattractive within 15 min of mating. However, when retested 2-3 and 24 h after mating, a significantly higher proportion of treated females regained their attractivity, while mated control females remained unattractive. This restorative effect was transient, though, as treated females retested 48 h after mating were as unattractive as the controls. Both anesthetized and control females were unreceptive when tested following mating and did not regain receptivity with time. Last, the mating-induced surge in circulating concentrations of prostaglandin was diminished in females that received a local anesthetic prior to mating. Taken together these results indicate that the loss of attractivity and receptivity following mating in the red-sided garter snake is due to combined effects of a mating pheromone and a physiological, neurally mediated response to the sensation of stimuli associated with the act of mating.     

Influence of androgen on the development of sexual behavior in rats : I. Time of administration and masculine copulatory responses, penile reflexes, and androgen receptors in females

The objective of the present study was to investigate the effect of the time of administration of androgen, during the neonatal period, on the development of masculine copulatory behavior in female rats. In addition, the influence of androgen, administered neonatally, on the development of penile reflexes and cytoplasmic androgen receptor levels in the hypothalamic-preoptic area (HPOA) was examined. Female rats were injected with 0.5 mg testosterone propionate (TP) at either 1, 8, or 24 hr after birth and again 24 hr after the first injection. Fifty percent of the females treated with TP at 1 and 8 hr after birth displayed the ejaculatory response when tested in adulthood. In contrast, 93 and 87.5% of oil-treated males and females, respectively, which were androgenized at 24 hr after birth exhibited this response. The results indicate that a considerable amount of masculinization occurs postnatally in the rat. However, none of the androgenized females displayed any penile reflexes even when tested following the display of an ejaculatory response. HPOA androgen receptor levels were somewhat higher in the oil-treated females than in males but were not correlated with the ability to exhibit ejaculation patterns.     

Prenatal stress reduces fertility of male offspring in mice, without affecting their adult testosterone levels

The male offspring of mice stressed by crowding during the final third of pregnancy showed reductions in sexual behavior and fertility. When paired with receptive females, their latencies to mount and to achieve intromission and ejaculation were greater than controls, and 30% of them failed to ejaculate in the 100-min test. When housed continuously for 4 days with females, 31% of them failed to impregnate their partners, compared with 4% of controls. The sexual receptivity of the untreated females paired with prenatally stressed males was not affected. Resting testosterone levels of prenatally stressed males did not differ from those of controls, and the pattern of rise and fall of testosterone during a 60-min interaction with a female showed only minor differences. The results suggest a central, rather than peripheral, mediation of the behavioral effects of prenatal stress.     

Androgen-induced alterations in vocalizations of femaleXenopus laevis: modifiability and constraints

Summary We examined effects of exogenous androgen (testosterone and dihydrotestosterone) on vocalizations of ovariectomized, adult female South African clawed frogs,Xenopus laevis. When paired with sexually active males, all ovariectomized females exhibited ticking, the unreceptive or release call. Ticking consists of low amplitude, regularly spaced clicks with a mean interclick interval of 154 ms. When androgen-treated and paired with sexually active males, these ovariectomized females also exhibited an aberrant call (atypical ticking) in which click multiples replaced the single clicks of ticking. Mean ICI's for atypical ticking were 37 ms for click doublets and 22 ms for click quadruplets. Androgen treatment decreased the total time spent vocalizing (typical and atypical ticking) by ovariectomized females.All androgen-treated females were then tested repeatedly with sexually receptive females in an attempt to elicit the male-typical vocalization, mate calling. Six of 17 females did not vocalize at all, even when gonadotropin injected. Eight females gave rapid (mean ICI, 36 ms) trains of clicks in an irregular temporal pattern (tick-like calls). Three females gave brief trills with alternating fast and slow components. Comparison of mate calllike vocalizations of androgen-treated females to mate calling of males reveals that calls in females are considerably shorter in duration (female: 0.32 min versus male: 45 min) and slower in tempo (ICI's; fast trill, female: 21 ms, male: 14 ms; slow trill, female: 36 ms, male: 28 ms). Incomplete masculinization of the vocal pattern of females by androgen treatment in adulthood may be due to developmental constraints on the modifiability of the neurons and muscles responsible for calling.Abbreviations C cholesterol - DHT dihydrotestosterone - HCG human chorionic gonadotropin - IBI interburst interval - ICI interclick interval - ovx ovariectomized - T testosterone     

Female Defensibility in a Small Troops of Japanese Macaques vis-à-vis Nontroop Males and Copulation on the Periphery of the Troop

I provide data compiled over 4 yr on the mating behavior in small troops of wild Japanese macaques on Yakushima Island. The key parameters are the number of sexually receptive females, the number of nontroop males (NTMs), and copulation on the periphery of the troop. I analyzed the following aspects: 1) changes in the proportion of copulation with high-ranking males (HRMs) and NTMs, 2) variations in factors such as fluctuation in the number of sexually receptive females and troop males and their effects on the number of visiting NTMs, 3) the effect of attempted interruption of mounting series by other males, and 4) some aspects of copulation on the periphery of the troop. Throughout the study, 56% of the total number of females mated most frequently with the α-male in a single mating season. However, the relative mating success of HRMs varied over the years and between individuals. The number of visiting NTMs varied depending on the number of receptive females and troop males. Females tended to mate with the NTMs when they appeared around their troops. The direct effect of interruption of the mounting series by other males is equivocal. The females mated with the low-ranking males (LRMs) and NTMs on the periphery of the troop, which increased the possibility of mounting series ending with ejaculation. Females actively sought opportunities for copulation on the periphery of the troop by moving there or initiating close proximity with LRMs and NTMs there. On Yakushima Island, the mating success of HRMs was not always as high as that predicted by the priority of access model. The injury status of the HRM, the number of visiting NTMs, and female choice are all considered to influence a male’s mating success.     

Genetic divergence and echolocation call frequency in cryptic species of Hipposideros larvatus s.l. (Chiroptera: Hipposideridae) from the Indo-Malayan region

The intermediate leaf-nosed bat ( Hipposideros larvatus ) is a medium-sized bat distributed throughout the Indo-Malay region. In north-east India, bats identified as H. larvatus captured at a single cave emitted echolocation calls with a bimodal distribution of peak frequencies, around either 85 kHz or 98 kHz. Individuals echolocating at 85 kHz had larger ears and longer forearms than those echolocating at 98 kHz, although no differences were detected in either wing morphology or diet, suggesting limited resource partitioning. A comparison of mitochondrial control region haplotypes of the two phonic types with individuals sampled from across the Indo-Malay range supports the hypothesis that, in India, two cryptic species are present. The Indian 98-kHz phonic bats formed a monophyletic clade with bats from all other regional populations sampled, to the exclusion of the Indian 85-kHz bats. In India, the two forms showed 12–13% sequence divergence and we propose that the name Hipposideros khasiana for bats of the 85-kHz phonic type. Bats of the 98-kHz phonic type formed a monophyletic group with bats from Myanmar, and corresponded to Hipposideros grandis , which is suggested to be a species distinct from Hipposideros larvatus . Differences in echolocation call frequency among populations did not reflect phylogenetic relationships, indicating that call frequency is a poor indicator of evolutionary history. Instead, divergence in call frequency probably occurs in allopatry, possibly augmented by character displacement on secondary contact to facilitate intraspecific communication.  © 2006 The Linnean Society of London, Biological Journal of the Linnean Society , 2006, 88 , 119–130.