Relation between the dominance rank of female rhesus monkeys and their access to males

Systematic observations were made on 12 measures of the sexual, aggressive, and social interactions of 24 male–female pairs of rhesus monkeys in six social groups, each consisting of one male and four ovariectomized females tested in a large room. Each female in a group was treated in turn first with estradiol alone and then with estradiol and progesterone in combination. When hormone-treated, the female was also observed during pair tests with the male in the same large observation room (four males, eight females, 240 group tests, 240 pair tests). The dominance ranks of females during group tests were determined post hoc by means of the dominance index [Zumpe & Michael, American Journal of Primatology 10:291–300, 1986]. In all six groups, the most dominant female virtually monopolized the male, and the subordinate females' interactions with the male, assessed during pair tests, were almost completely suppressed during group tests. This “dominant female effect” was a robust phenomenon that depended solely on female dominance rank. It was independent of the identity and hormonal status of females and of the social preferences of males as expressed in pair tests. These findings demonstrate the existence of female mate competition in an Old World primate.     

Effects of ovarian hormones on the behavior of captive Macaca fascicularis

To examine the effects of ovarian hormones on the behavior of female Macaca fascicularis and their male partners, daily 1-hr behavior tests were conducted while ovariectomized females were (1) untreated, (2) given estradiol benzoate (EB) (5 μg subcutaneously [s.c.]/day), (3) given estradiol benzoate together with increasing doses of progesterone (P) (5 mg, 10 mg, and 20 mg. s.c./day), and (4) given testosterone propionate (TP) (0.25 mg s.c./day) (six pairs, 540 tests). Weekly blood samples were analyzed by radioimmunoassay for plasma hormone levels (81 samples). Estrogen treatment produced plasma estradiol levels similar to those of intact females during the late follicular phase of the menstrual cycle. Additional progesterone at the lowest dose produced plasma progesterone levels similar to or somewhat higher than those during the midluteal phase, while higher doses produced supraphysiological levels. Androgen treatment resulted in plasma levels well above the physiological range. Hormone treatments produced highly significant effects on the sexual, social, and aggressive interactions of the pairs. As in rhesus monkeys, estrogen increased male and female sexual activity, and increasing doses of additional progesterone reversed these effects. Unlike in rhesus monkeys, testosterone propionate increased both female sexual motivation (invitations) and also male sexual activity and ejaculatory performance. The direction of the hormone-dependent changes in grooming and aggressive interactions confirmed earlier results with intact females and indicated that aggressive interactions and male grooming times were highest, and female grooming times were lowest, when copulatory activity was at its height.     

Sexual preferences during artificial menstrual cycles in social groups of rhesus monkeys (Macaca mulatta)

Eight groups of rhesus monkeys each consisting of one male and four ovariectomized females were observed while two of the females were treated with hormones to produce artificial menstrual cycles. These were either synchronized or offset by 7-day increments. Sexually preferred females, defined by the numbers of ejaculations per test, received almost twice as many ejaculations as did non-preferred females during all synchronized and offset cycles and during all cycle phases. However, short-term changes in partner preference occurred when the midcycle phase of non-preferred females coincided with the middle or late progesterone phase of preferred females, suggesting a negative effect of progesterone on behavior during the menstrual cycle. There were highly significant differences between preferred and non-preferred partners for almost all of their sexual and social interactions, and preferred partners showed longer proximity and grooming times as well as higher levels of sexual activity. Partner preferences accounted for more of the behavioral variance between pairs than did female dominance, although males sought the proximity of dominant females independently of their partner preferences. Thus, in a setting uncomplicated by male mate competition, sexual preference by male rhesus monkeys is a robust phenomenon depending on complex interactions between dominance, hormonal status, and the individual behavior of female partners.     

Sexual behavior and hormone levels during the menstrual cycles of rhesus monkeys.

The sexual interactions of 10 pairs of rhesus monkeys were observed during a control and an experimental menstrual cycle of each female. During the experimental cycle the females were treated with an antiandrogen, flutamide. Daily peripheral serum levels of estradiol, testosterone, and progesterone in each female were determined by radioimmunoassay. Sexual behavior did not correlate reliably with female serum concentrations of any hormone measured nor with the menstrual cycle stage. Administration of the antiandrogen to the females did not affect the sexual behavior of the pairs, although female serum levels of estradiol and testosterone were reduced. It was concluded that although female ovarian hormones may influence rhesus sexual interactions under some circumstances, the normal hormonal fluctuations during the menstrual cycle need not regulate this behavior; a knowledge of an intact rhesus female's hormonal condition does not allow accurate predictions about behavior displayed during laboratory pair tests with a male.     

Ejaculation by male rhesus as a function of the female partner

Nine adult male rhesus monkeys were given eight 10-min tests of sexual behavior with eight ovariectomized female rhesus pretreated with estradiol benzoate. Males differed significantly in the number of tests during which they ejaculated, and females differed in the frequency with which specific males ejaculated when tested with them. With phylogenetic increase in neocortex, pair compatibility may be as important as hormonal stimulation in regulating male sexual performance. If this is correct, the problem of understanding the determinants of primate sexual behavior becomes more formidable.     

Natural or hormone-induced sexual and social behaviors in the female brown lemming (Lemmus trimucronatus)

The behaviors of intact or ovariectomized, estradiol benzoate-treated or estradiol benzoate followed by progesterone-treated female brown lemmings were compared. Intact, diestrous females engaged in more social interactions with a male than did ovariectomized females (Experiment 1). In the first 5 min of a 1-hr mating exposure (Experiment 2, Test A) intact females in natural estrus engaged in more social and sexual behaviors than did ovariectomized females in estrogen-induced estrus. However, during the last 5 min of the 1-hr exposure (Test B) ovariectomized females receiving estrogen alone continued to show high levels of sexual activity with a male partner, while intact estrous females or females receiving estrogen followed by progesterone showed an apparent drop in sexual receptivity and an increase in aggressivity. Aggressive behaviors, as indexed by threat-leap behaviors on the part of the female may increase in the presence of progesterone. Declines in sexual activity, occurring within 1 hr of progesterone injection, were apparently dependent on the interaction of progesterone and copulatory events which may affect both the male and female.     

Social and hormonal influences on behavior of adult male, female, and pseudohermaphroditic rhesus monkeys

We previously demonstrated that in a simple pair test situation the expression of adult male sexual behavior by rhesus monkeys depends on both prenatal (organizational) and adult (activational) androgen exposure. In the present study we used a more complex social situation (trio tests) to evaluate the behavior of males, females, and female pseudohermaphrodites. In these trio tests, the experimental subjects were tested with two estrogenized stimulus females simultaneously. Sex differences in behavior were made apparent by this complex testing situation that could not have emerged in the pair test. Gonadectomized males and female pseudohermaphrodites, but not ovariectomized females that were concurrently receiving TP, exhibited increased male sexual behavior in trio tests compared to pair tests. In trio tests, the males and pseudohermaphrodites showed evidence of partner preference by interacting almost exclusively with one of the two stimulus females. These "preferred females" in turn were responsible for the majority of the proceptive behavior exhibited in these tests. Ovariectomized females rarely displayed male sexual behavior in either test situation. These results further support the hypothesis that prenatal androgen exposure predisposes monkeys to exhibit masculine behavior traits when they reach adulthood and are exposed to the activational influences of androgens.     

Increases in testosterone levels and in copulatory behavior of male rhesus monkeys following treatment with human chorionic gonadotrophin

The sexual behavior of five male rhesus monkeys was observed before, during, and after administration of human chorionic gonadotropin (HCG) sufficient to induce increases in serum testosterone. Each male was given 12 half-hour pair tests with an estrogen-implanted ovariectomized female during each of the three phases of the study (Pretreatment, Treatment, Post-treatment). Summaries of selected categories of sexual and other social behaviors were tabulated for each phase of the study. Grooming, mount latency, and ejaculation frequency, as well as other behavioral measures, were unaffected by hormone treatment. However, latency to ejaculation decreased by 40% (P < 0.01) and mount rate increased by 71% (P < 0.05) during hormone administration. Sexual presentations by the female decreased by 38% (P < 0.05). Limb shaking decreased 55% during HCG treatment (P < 0.05). These findings demonstrate that increases in testosterone secretion subsequent to gonadotrophin injection in intact male rhesus monkeys can produce significant alterations in male and female sexual behavior.     

Behavioral effects of a synthetic mixture of aliphatic acids in rhesus monkeys (Macaca mulatta)

The stimulation of sexual behavior by a synthetic mixture of volatile aliphatic acids (acetic, propanoic, methylpropanoic, butanoic, methylbutanoic, methylpentanoic) was studied in male rhesus monkeys. Twelve intact adult males and 12 long-ovariectomized adult females were used in 24 paired combinations (541 tests each of 1 hr). A mixture of authentic acids similar to that found in the vaginal secretions of estrogenized females was applied to the sexual skin area of ovariectomized females immediately before tests with males. There was marked between-pair variability during the application of both control and test substances. However, using rigorous behavioral criteria, there was a well-marked stimulation either of male mounting attempts or of ejaculations in 12 of 24 pairs involving 9 of 12 males. Three males responded with both female partners, three responded with neither female partner, and six responded with one partner only. In the responding pairs, there were highly significant increases in mounting attempts and ejaculations, an effect that could be attributed only to treatment. We conclude, therefore, that these aliphatic acids (copulins), which act via olfactory pathways, have communicatory significance in rhesus monkeys.     

Role played by the ovary and adrenals in early receptivity during 4-day cycle in the female rat

The mechanisms involved in the control of precocious sexual receptivity were studied in 4-day cyclic female Wistar rats injected with 10 μg estradiol benzoate (EB) and caged with a male during the night from diestrus II to proestrus. Early mating frequencies were compared in intact females, in animals ovariectomized on the morning of diestrus I, in adrenalectomized and in adrenalectomized-ovariectomized females. No change in early sexual receptivity occurred either in ovariectomized, or in adrenalectomized animals. On the contrary, a significant decrease of precocious mating frequencies was noted in adrenalectomized-ovariectomized females. The role played by the ovary in the control of precocious receptivity was supposed to be due to the secretion of progesterone which has been evidenced on the late afternoon of diestrus II in estrogen treated females.Concerning the mechanisms by which the adrenals may compensate for the ovaries in the control of early sexual receptivity in estrogen-primed females it was observed that notwithstanding an inhibitory action exerted by EB on the adrenal progesterone secretion, a low rate of progesterone was maintained in the peripheral plasma which was compatible with early mating in ovariectomized animals.     

Relation between the hormonal status of the female and direct and redirected aggression by male rhesus monkeys (Macaca mulatta)

Each of 16 feral-reared male rhesus monkeys was paired with an ovariectomized female (8 females) during daily 60-min behavior tests (16 pairs). Each male received 8 consecutive tests with an untreated female, 8 tests when the female received injections of estradiol, and finally 8 tests after estrogen was withdrawn (total, 384 tests). Of the 16 males, 11 threatened sufficiently often for numerical analysis (“aggressive” males). Two of these males showed no changes either in sexual activity or in agonistic behavior when the females were estrogenized. In the remaining 9 males, there was increased sexual activity when the females were estrogenized and this was associated with a significant decrease in direct aggression (P < 0.01) and an increase in redirected aggression (P < 0.05). The demonstration in the same males of an inverse relation between threats directed toward and away from the female supports the hypothesis that threats directed away from the sexual partner represent aggression aroused by the partner that is redirected onto the environment when sexual interest increases.     

Behaviorial effects of a synthetic mixture of aliphatic acids in rhesus monkeys (Macaca mulatta).

The stimulation of sexual behavior by a synthetic mixture of volatile aliphatic acids (acetic, propanoic, methylpropanoic, butanoic, methylbutanoic, methylpentanoic) was studied in male rhesus monkeys. Twelve intact adult males and 12 long-ovariectomized adult females were used in 24 paired combinations (541 tests each of 1 hr). A mixture of authentic acids similar to that found in the vaginal secretions of estrogenized females was applied to the sexual skin area of ovariectomized females immediately before tests with males. There was marked between-pair variability during the application of both control and test substances. However, using rigorous behavioral criteria, there was a well-marked stimulation either of male mounting attempts or of ejaculations in 12 of 24 pairs involving 9 of 12 males. Three males responded with both female partners, three responded with neither female partner, and six responded with one partner only. In the responding pairs, there were highly significant increases in mounting attempts and ejaculations, an effect that could be attributed only to treatment. We conclude, therefore, that these aliphatic acids (copulins), which act via olfactory pathways, have communicatory significance in rhesus monkeys.     

A review of sexual initiating behavior by male and female cynomolgus monkeys and some species comparisons

The sexual initiating behavior of male and female cynomolgus monkeys (Macaca fascicularis) observed during standard laboratory tests is reviewed and compared with that of rhesus monkeys (M. mulatta) observed under identical conditions. Species differences in sexual behavior are related here to differences in habitat, sexual dimorphism, and the dominance gradient between the sexes. Compared with rhesus monkeys, cynomolgus monkeys appear to be more arboreal, less sexually dimorphic, and have a smaller dominance gradient between the sexes. They exhibit a facultative single-mount copulatory pattern rather than the serial mount pattern of the rhesus monkey. Female cynomolgus monkeys are less dominated than rhesus females by their male partners. Direct aggression between mates is more frequent and redirected aggression occurs less often than in rhesus monkeys. These behavioral differences affect the interpretation of changes in initiation rates that occur (1) during the menstrual cycle, (2) when females are ovariectomized and given hormone replacement treatments, and (3) when males are castrated and treated with androgens. We conclude that estradiol in the female and testosterone in the male increase the sexual motivation of both the treated and the untreated partner. Valid interpretations of changes in initiation rates depend on accurate and exclusive definitions of behavior and on a consideration of the behavioral context in which they are made.     

Proceptive behavior of female rhesus monkeys during tests with tethered males

Proceptive behavior of female rhesus monkeys during follicular and luteal phases of the ovarian cycle was examined in laboratory tests with a tethered male partner. Cyclical changes in proceptive behavior were observed. In tests during the follicular phase of their cycles, females on the average approached and solicited the male at a higher rate, spent more time sitting within proximity of him, and less time at a maximum distance away from him than during tests in the luteal phase of their cycles. Additionally, in the follicular phase of their cycles, females exhibited an increase in proceptivity following the male's ejaculation. This latter finding was discussed in light of other observations demonstrating that male rhesus monkeys are capable of multiple ejaculations. When females were paired with a tethered, ovariectomized female as a partner, rather than an adult male, none of the cyclical changes in proceptive and sexual behavior were observed.     

Female-typical sexual behavior of rhesus and defeminization by androgens given prenatally

Adult rhesus monkeys were observed in standardized tests for female-typical sexual and related social responses. In the first experiment reported, 7 castrated males and 5 spayed females were paired with each of 4 intact males on two occasions following intramuscular injection with estradiol benzoate (EB) (6 micrograms/kg X 14 days) and on two other occasions without such treatment. In tests without EB, males and females did not behave differently toward the intact male partners, and all responses were displayed at low frequencies. In tests with EB, females showed reliably higher frequencies than males of approaching, sitting close to, grooming, and soliciting, and they presented to a higher proportion of the male partner's sexual contacts. EB reliably increased the frequency of display of all of these same five responses in females but not in castrated males. The intact male partners displayed reliably fewer approaches, sexual contacts, mounts, intromissions, and ejaculations to castrated males than to spayed females regardless of estrogenization. In a second experiment 10 intact adult pseudohermaphroditic females and 6 intact control females were tested following EB injections with each of the same 4 intact males. Pseudohermaphrodites were experimentally produced by injecting pregnant females with either testosterone propionate (TP) or dihydrotestosterone propionate (DHTP). Pseudohermaphrodites, regardless of type of androgen used in their production, showed reliably fewer solicits than controls to male partners. Moreover, they displayed most of the other responses at lower average frequencies than controls. Frequencies of intromission and ejaculation by intact male partners were reliably lower with pseudohermaphrodites than with control females, but frequencies of approach, sexual contact, and mount were not reliably different. We conclude that in this testing and measurement situation male and female rhesus monkeys differ markedly in the degree of expression of female-typical sexual behaviors, and genotypic males are behaviorally less responsive to estrogens than females. Exposing genotypic females to androgens during fetal life decreases the expression of female-typical, estrogen-influenced responses, and the effect is most pronounced on those soliciting responses that subserve proceptivity.     

Hormones and social behavior of squirrel monkeys. (Saimiri sciureus). I. Effects of endocrine status of females on behavior within heterosexual pairs.

Intact male squirrel monkeys were paired with ovariectomized females given either oil vehicle, estradiol benzoate (10 μg) alone, or estradiol benzoate combined with progesterone (5 mg). Affiliative behaviors, including social contacts, female grasping of the male, male and female approaches, and following by the male were observed more frequently, and social distance decreased when females received estradiol as compared to oil. Furthermore, when progesterone was combined with estradiol, some of the effects seen with estradiol alone, such as grasping by the female and following by the male, were reversed. These results support the hypothesis that seasonal changes between sex-segregated and sex-integrated forms of social organization reported for this species are influenced by endocrine conditions of the female.     

Differential hormonal control of aggression and sexual behavior in female Syrian hamsters

These experiments were designed to test the effects of chronic estradiol treatment on aggression and sexual behavior in female hamsters. Isolated female hamsters were ovariectomized and tested for their behavioral responses to a group-housed, ovariectomized female hamster (aggression test) and a group-housed, intact male hamster (sexual behavior test). Following these baseline tests, the experimental females were implanted sc with Silastic capsules containing different concentrations of estradiol (100, 25, 10, or 0%) diluted with cholesterol and retested 3, 7, 10, and 14 days after implantation. High levels of aggression were observed on the baseline test, with no changes in aggression toward an intruder female observed for any implant group on subsequent tests. Despite these high levels of aggression toward another female, most of the estradiol-treated females (80% at 14 days) were sexually responsive in the presence of a male. There was no effect of Silastic estradiol concentration on sexual behavior, even though a range of serum estradiol levels (39–105 pg/ml) resulted. Lordosis latencies decreased and lordosis durations increased over the extent of estradiol treatment. Seventeen days after Silastic implantation, all females were injected with progesterone and retested. Estradiol-treated females showed an extreme reduction in aggression toward a stimulus female, as well as a further stimulation of sexual behavior after progesterone treatment. High levels of aggression in cholesterol-treated females (0% estradiol) were maintained even after progesterone injection, and these females never displayed any sexual responsivity. These results suggest that sexual behavior in the female hamster is sensitive to estradiol alone, whereas the inhibition of aggression requires the combination of estradiol plus progesterone.     

Seasonal changes in reproductive behavior in two ovariectomized female rhesus monkeys treated year-round with estradiol

Two ovariectomized female rhesus monkeys treated year-round with estradiol-filled capsules were used in hour-long behavioral tests with male rhesus monkeys both in and out of the normal breeding season. The study was designed primarily to test male hormonal responses to copulatory behavior and it was expected that behavior of the females would be essentially the same under both seasonal conditions. Several behaviors of the female, however, were found to fluctuate on a seasonal basis, namely (1) proximity to the male, (2) grooming of the male, (3) sexual presentations, and (4) threatening away (a form of sexual invitation). All of these behaviors, except proximity, were found to be positively correlated with the male partner's testosterone levels before and after the behavior test in the only test condition in which most males ejaculated. The preliminary suggestion is made that these females responded to some cue, either from the environment or from the males, that caused a change in their behavior between breeding and nonbreeding seasons despite the constant hormonal environment provided by the estradiol capsules. Since the same behaviors which were sensitive to seasonal effects were positively correlated with male testosterone levels, it is possible that the male's hormonal status affects affects female behavior.     

Estrogen and progesterone interactions influencing sexual and social behavior in the brown lemming, Lemmus trimucronatus.

The effects of estrogen and progesterone on the social and sexual behavior of brown lemmings, Lemmus trimucronatus, were investigated. The behavior of hormone-treated and untreated ovariectomized females and sexually vigorous males was observed in six consecutive daily 5-min dyadic encounters. Sexual receptivity, as measured by lordosis, and other social behaviors including nasonasal contact, boxing postures, allogrooming, perineal investigation, and male mounting increased following 48 hr of exposure to daily injections of 0.5 μg estradiol benzoate (EB). Lordosis in EB-primed females was not facilitated or inhibited by short-term (4 hr) exposure to 0.5 mg progesterone (P). Long-term (greater than 24 hr) exposure to P apparently inhibited lordosis and other social behaviors in EB-treated females, although males continued to attempt to mount these females. In EB-treated females a dramatic increase in threat-leaps, directed by the female toward the male, was observed within 4 hr of P injection. Threat-leaps declined when P was withdrawn. Threat-leaps were also observed in ovariectomized females after prolonged exposure to P only (0.5 mg/day). Vaginal perforation and cornification were first apparent 48 hr after EB injection. P-alone treated ovariectomized females also showed vaginal perforation but cornified cells were infrequent and these animals did not show lordosis.     

Mu-, delta-, and kappa-opioid receptor agonists selectively modulate sexual behaviors in the female rat: differential dependence on progesterone.

Previous studies suggested that opioid receptor agonists infused into the lateral ventricles can inhibit (through mu receptors) or facilitate (through delta receptors) the lordosis behavior of ovariectomized (OVX) rats treated with estrogen and a low dose of progesterone. The present study investigated the behavioral and hormonal specificity of those effects using more selective opioid receptor agonists. Sexually experienced OVX rats were implanted stereotaxically with guide cannulae aimed at the right lateral ventricle. One group of rats was treated with estradiol benzoate (EB, 10 micrograms) 48 hr and progesterone (P, 250 micrograms) 4 hr before testing, whereas the other group was treated with EB alone. Rats were infused with different doses of the selective mu-receptor agonist DAMGO, the selective delta-receptor agonist DPDPE, or the selective kappa-receptor agonist U50-488. The females were placed with a sexually vigorous male in a bilevel chamber (Mendelson and Gorzalka, 1987) for three tests of sexual behavior, beginning 15, 30, and 60 min after each infusion. DAMGO reduced lordosis quotients and magnitudes significantly in rats treated with EB and P, but not in rats treated with EB alone. In contrast, DPDPE and U50-488H increased lordosis quotients and magnitudes significantly in both steroid-treatment groups. Surprisingly, measures of proceptivity, rejection responses, and level changes were not affected significantly by mu or kappa agonists, although proceptivity and rejection responses were affected by DPDPE treatment. These results suggest that the effects of lateral ventricular infusions of opioid receptor agonists on the sexual behavior of female rats are relatively specific to lordosis behavior. Moreover, the facilitation of lordosis behavior by delta- or kappa-receptor agonists is independent of progesterone treatment, whereas the inhibitory effect of mu-receptor agonists on lordosis behavior may require the presence of progesterone.