Declines in sociosexual behavior in golden monkeys (Rhinopithecus roxellana): Associated environmental and social variables

Between February 22 and August 10, 1986, 200 h of systematic observation were conducted on a male and female golden monkey (Rhinopithecus roxellana) at Seattle's Woodland Park Zoo and Portland's Washington Park Zoo. The pair was moved to Portland on May 6, and on July 24 the female unexpectedly gave birth to a male infant, the first such birth in the United States. Dramatic behavioral changes occurred immediately after the pair was moved to Portland, the midpoint of the female's pregnancy, including the disappearance of sexual behavior and a sharp decline in time spent in contact. Explanations for these changes are discussed.     

The reproductive behavior of golden monkeys in captivity (Rhinopithecus roxellana roxellana)

The reproductive behavior of two captive harem breeding groups of golden monkeys was observed over one mating season and compared to non-seasonal reproductive behavior. Observation of over two thousand sexual interactions suggests that 1) females were responsible for 95% of all sexual solicitations (proceptive behavior), of which the typical pattern was prostration, while males were responsible for only 5%; 2) 17% of female solicitations were interrupted by another female; 3) 52% of female solicitations resulted in mounting by males; 4) the frequencies of solicitations and receipt of mounts and ejaculations varied greatly among females; 5) the frequency of ejaculations, the ratio of ejaculations to mountings, and ejaculation patterns were different between two males, and 6) the golden monkey is a seasonal breeding animal.     

Vocal communication in captive golden monkeys (Rhinopithecus roxellanae)

The Sichuan golden snub-nosed monkey,Rhinopithecus roxellanae, is an endangered Colobine endemic to China. The behavior and biology of this species are little known, and it has rarely been kept in captivity outside China. Results from 42 hr of observations of a male-female golden monkey pair provide preliminary information on the vocal behavior of this species in captivity. Vocalizations by the animals often occurred within antiphonal sequences, which were primarily initiated by the female. Sequences were brief (2–3 calls), showed little or no temporal overlap, and were emitted primarily when the animals were distal from one another, suggesting that sequences may function as contact calls in nature. Some vocalizations appeared to be cryptic, i.e. unaccompanied by mouth or body movement, and these were observed more often than noncryptic calls in both animals. Vocal communication appears to be complex in this species, and remains poorly understood.     

Pretreatment with CP-154526 blocks the modifying effects of alarm pheromone on components of sexual behavior in male, but not in female, rats

We previously demonstrated that an alarm pheromone released from male donor Wistar rats evoked several physiological and behavioral responses in recipient rats. However, the pheromone effects on social behavior were not analyzed. In the present study, we examined whether the alarm pheromone affects sexual behavior in male or female rats. When a pair of male and female subjects was exposed to the alarm pheromone during sexual behavior, the ejaculation latency was elongated, the number of mounts was increased, and the hit rate (number of intromissions/number of mounts and intromissions) was decreased in the male subject. In contrast, female sexual behavior was not affected by the alarm pheromone. When we exposed only the male or female subject of the pair to the pheromone just before sexual behavior, the results were similar: the pheromone effects were evident in male, but not in female, subjects. In addition, when we pretreated with corticotropin-releasing factor (CRF) antagonist (CP-154526) before exposing the male subject to the alarm pheromone, the pheromone effects were attenuated in a dose-dependent manner. These results indicate that the alarm pheromone modifies male, but not female, components of sexual behavior and that CRF participates in the effects.     

Relationship between male-male and male-female sexual behavior in 5-6-month-old male lambs

To characterize male–male sexual behavior during lamb development, to relate it with lamb body and testicular growth, and with sexual behavior toward estrual ewes, 40 Milchschaf male lambs, weaned at 45 days of age, were kept with ewes that were nursing younger lambs. Experimental lambs were weighed and scrotal circumference was measured every 2 weeks. Male–male sexual behavior was observed during 1–2 h every 2 weeks after birth until 7 months of age. Observations were recorded more intensively (3–4 h on five different days) for 2 weeks (5–6 months of age) as male–male sexual behavior increased during that period. Both mounting and mounted lambs were identified. An individual mounting index (MI) was calculated. To study male–female sexual behavior, lambs were individually located with two estrual ewes, and during 5 min the number of ano-genital sniffing, lateral approaches, mounts, and mounts with ejaculation were recorded. From those data, a libido index was also calculated. Male–male mounts (n = 308) were observed. Courtship behavior was displayed in 25% of interactions; mounts were accepted in 72.1% of attempted mounts. Mounts without previous courtship were accepted more frequently than mounts with previous courtship (P = 0.002). Lamb weight and scrotal circumference were not different according to MI groups. Lambs that mounted more times estrual ewes (first tertile) had greater (P = 0.04) MI (0.61 ± 0.10) than lambs with medium (0.27 ± 0.09) and less (0.30 ± 0.10) MI. The regression between MI and heterosexual libido index was r = 0.33 (P < 0.05). In summary, intensive male–male sexual activity during a short period of male lamb development was observed. There was a positive relationship between sexual behavior of male lambs towards other male lambs and towards estrual ewes.     

Hormonal and social factors affecting evoked sexual behavior in Rhesus monkeys

Male rhesus monkey sexual behavior occurring spontaneously or evoked by remotely-controlled hypothalamic stimulation was studied in dominant and subdominant males with both dominant and subdominant, estrogen-treated or untreated, ovariectomized females. The behavior was quantified in terms of number and duration of ejaculatory sequences, number of thrusts, and number of mounts per sequence. Little or no spontaneous sexual behavior was observed with an untreated ovariectomized female. However, evoked sexual behavior with the exception of evoked ejaculation could be obtained whether the females were treated or untreated. Spontaneous and evoked sexual behavior was directed towards both dominant and subdominant females. The female chosen by the male was in part determined by the dominance status of the female. Evoked sexual behavior differed from spontaneous behavior in terms of an increased number of thrusts per mount, an increased number of ejaculations per session, and a decrease in latency between ejaculatory sequences.     

人工饲养下金丝猴繁殖的观察研究 Ⅰ.交配行为

金丝猴(Rhinopithecus roxellanae)是我国稀有的珍贵特产动物,笔者在多年观察金丝猴的繁殖行为的基础上,又于1986年8-9月在北京动物园,对金丝猴的交配、爬跨行为进行了专门观察,发现金丝猴发动性活动的一些特点,并在交配爬跨时,雄性金丝猴有卷尾现象。其交配行为与叶猴和猕猴有差异。     

Wooing during Day or Night is not the Same: an Experimental Study in the Wolf Spider Schizocosa malitiosa

Diurnal and nocturnal activity patterns shown by different species will strongly determine the characteristics of signals as well as the sensory channels used during sexual interactions. Despite this, few studies have experimentally tested the effects of lighting and time of day on courtship characteristics in arthropods. Previous studies have shown that the wolf spider Schizocosa malitiosa can be active during the day or at night. We tested whether the period of the day affects the sexual behavior of S. malitiosa, by pairing males and females under diurnal or nocturnal conditions. We carried out mating trials in diurnal and nocturnal conditions in arenas containing female refuges. In diurnal conditions, male leg shaking behavior occurred at higher rates and consisted of greater leg raising angles relatively to nocturnal conditions. We did not find differences in mounts and mount latency between both experimental groups. In nocturnal conditions, female attacks and emergence from refuges were higher. Also, although mount occurrence did not differ between the two treatments, mounts inside the refuge were more frequent in diurnal conditions. Results suggest behavioral flexibility in male courtship and female receptivity responses relative to the time of the day.     

Observation on mating behavior and sexual play in the squirrel monkey (Saimiri sciureus)

Behavior patterns during play, sexual role differentiation dependant on age, and mating behavior in squirrel monkeys living in laboratory groups are described. While juveniles prefer mutual play (wrestling, contact play) adults or subadults most often use distinct roles at play; the male acts as the pursuer and the female flees but provokes his further pursuit. The male usually initiates the interaction by approaching, while the female determines what course it will follow (retreating or play or mating). True copulatory behavior occurs in a rather stereotyped manner. A sequence of 10–25 mounts with rapid, followed by slow and intense pelvic thrusts, terminates with ejaculation. Mounts with or without rapid thrusts may occur during play, but long series of slow thrusts characterize mating behavior. Between the mounts the female repeatedly displays genitals to the male and both partners purr to each other. An increase of urine washing and genital inspection may be observed but is not restricted to days when mating occurs. The influence of rank order among males on sexual behavior is discussed.     

Mating behavior and male mating success in wildAnastrepha Ludens (Diptera: Tephritidae) on a field-caged host tree

Mating behavior and factors affecting mating success of males were studied using wild Anastrepha ludens on a fieldcaged host tree. The most common courtship sequence had five components: (1) male calls from the underside of a leaf, (2) female arrives to the maleoccupied leaf, (3) male orients to female and stops calling, (4) one or both approach to a face-to-face position 1–3 cm apart, and (5) male mounts female after 1–2 s. Courtship behavior was almost identical to that of laboratoryculture flies observed previously under laboratory conditions. Most malefemale encounters occurred at a height of 1–2m, well inside the outer canopy of the tree. Differential mating success by males occurred. No male mated more than once per day, owing possibly to a very short sexual activity period. Factors favoring mating success of males were survival ability and tendency to join male aggregations and to fight other males. Thorax length and age (9–11 days difference) had no effects on male copulatory success. Overall win/loss percentage was not related to mating success because the males that were most successful at mating fought mostly among themselves, driving their win/loss percentage down. However, these successful males (at mating) won most of their fights against less successful males. Results confirmed a lek mating system: males aggregated, called, and defended territories; territories did not contain femalerequired resources; and females exercised mate choice, apparently through selection of sites within leks.     

Male aggression during mating: evidence for sexual coercion in a female dominant primate?

In this article we document male sexual coercion of a Lemur catta female on St. Catherines Island (SCI), USA. Data presented in this paper were collected on one free-ranging L. catta group during October-November 2002 using all-occurrences sampling for agonism and reproductive behavior. We observed a male forcefully attempting to mate with a year-old estrous female. Despite the fact that we observed this female to present to the male during her estrus, throughout the episode the male employed the use of force, and achieved penile intromission on at least one occasion while the female struggled and resisted. We interpret his behavior as sexual coercion. As measured by sexual presents, the female appeared to more strongly prefer two other males as mates, yet each of these males gained fewer mounts and less cumulative time spent in mounts than the coercive male. The coercive male was one of two group males with the lowest observed mating success, suggesting that coercion might be a strategy used by males who are not highly sexually preferred. Females undergo early sexual maturation at this site owing to provisioning, and can therefore enter estrus before fully attaining dominance over males. As such, these data suggest that one consequence of provisioning a wild L. catta population (or of maintaining L. catta in captivity) may be that young females can be the targets of sexual coercion if they reach sexual maturity before fully achieving social dominance over males. In conclusion, male sexual coercion can occur in L. catta despite the female dominance characteristic of this species, and can constrain the mating behavior of females.     

Sexual initiation in wild mountain gorillas

A field study of wild mountain gorillas was conducted to elucidate details of sexual initiation required for an interpretation of the increased frequency of copulation during the menstrual cycle, in comparison to the wild, that occurs when this species is tested in traditional laboratory pair tests. Although females in the wild played a clear role in establishing and maintaining proximity to the male and assertively presenting for copulation, all female presenting was preceded by some form of behavior by the male. Of particular relevance were several components of the male’s chest-beat display that had been observed at much higher frequencies in the laboratory tests. Although originally described as male aggression in the laboratory tests, such behavior now appears to be male sexual initiative, elicited by female proximity. The exaggerated form and frequency of the display in the laboratory, and the increased copulation during the cycle that ensued, are likely due to (1) placing females in proximity to a male daily, rather than on 2–3 days of estrus as occurs in the wild, and (2) the inability of the female in the laboratory to withdraw from male proximity during pair tests in a single cage. In addition to clarifying the data on laboratory pair tests, the data on wild gorillas have relevance to the captive breeding of gorillas.     

Sexual behavior in a one-male unit of Rhinopithecus bieti in captivity

Data regarding the sexual behavior of black-and-white snub-nosed monkeys (Rhinopithecus bieti) were collected in 1998 in a one-male unit in captivity by all-occurrences sampling during the mating season. Before the present study, little was known about the sexual behavior of this species. This study showed that female solicitation is mainly expressed as “prostration plus glancing laterally” (PG) or “sitting plus head moving up and down” (HM), and male solicitation is exhibited by the “grunt bared-teeth display.” The mount-to-ejaculation ratio was 5.2 on average, and single-mount ejaculations (SMEs) were observed in only 4.4% of mounts on days with at least one ejaculation. Therefore, the main copulatory pattern of this species is multiple-mount ejaculation (MME). Females initiated 72% of 18 ejaculatory mounts. Females initiated more ejaculatory mounts than non-ejaculatory ones. In general, the patterns of sexual behavior in this species are similar to those reported for other Colobines. Zoo Biol 23:545–550, 2004. © 2004 Wiley-Liss, Inc.     

Mating patterns in the golden lion tamarin (Leontopithecus rosalia): continuous receptivity and concealed estrus

Sociosexual behavior was monitored on a daily basis for 3 months in 5 pairs of golden lion tamarins (Leontopithecus rosalia). Urine samples were collected daily from each female and urinary estrogen cycles were determined by radioimmunoassay. Mounts and copulations were observed during all phases of the estrogen cycle. Peaks or regular cycles in sexual behavior were not documented. There were no significant changes in affiliative behavior by females or males that were associated with changes in urinary estrogen values. A negative relationship between pair bond duration and frequency of sexual interactions was observed: newly established pairs exhibited 2-6 times more frequent sexual behavior than a long-established pair. The lack of a conspicuous sexual signal in female golden lion tamarins may be related to a pattern of continuous sexual receptivity. Both reproductive patterns, concealed estrus and continuous receptivity, are explicable in relation to either monogamous or polyandrous mating systems.     

Changes in Social Behavior and Their Hormonal Correlates during Pregnancy in Pig-tailed Macaques

I conducted a longitudinal study of hormones and social behavior during pregnancy in 8 female pig-tailed macaques (Macaca nemestrina) living in a captive social group. Females exhibited reduced grooming activity after the first month of pregnancy and reduced aggressiveness in the last month. Female-male hindquarter presentations and male-female foot-clasp mounts decreased steadily during pregnancy. The week before parturition was associated with lower involvement in all social activities. Monthly changes in plasma concentrations of estradiol and progesterone are correlated with some changes in sexual behavior and grooming performed by pregnant females. Altogether, the findings suggest that pregnancy does not bring about a major disruption of female social relationships with other group members and that the influence of pregnancy hormones on female affiliative and agonistic behavior is less marked than that previously observed for infant-directed behavior.     

Non‐Conceptive Sexual Behavior in Spiders: A Form of Play Associated with Body Condition,Personality Type,and Male Intrasexual Selection

In the socially polymorphic spider Anelosimus studiosus, males mature early in the reproductive season and recruit to the webs of juvenile females and guard them until they mature. During the period before females mature, males and females engage in repeated bouts of non‐conceptive (play) sexual behavior, where the pair courts and engages in mock copulation; both males and females gain performance‐enhancing experience via these encounters. In this study, we examined the factors that underlie individual variation in the tendency to engage in non‐conceptive mating and determine whether it impacts male–male competition for females. We found that docile females, being less resistant to mating in general, are more likely to accept male courtship and non‐conceptive copulation as juveniles. Personality type influenced the exhibition of non‐conceptive sexual behavior in males as well. High body condition males of the aggressive phenotype were more likely to engage in non‐conceptive sexual behavior than males with lower body condition. Body condition did not influence docile males’ propensity to engage in non‐conceptive sexual behavior, but female size did. Docile males engaged in more non‐conceptive sexual displays with larger females. Engaging in non‐conceptive sexual displays negatively impacted male performance in staged male–male contests for access to females. This cost was greatest for males of the aggressive phenotype, which are otherwise favored in male–male contests. Our findings indicate expression of non‐conceptive sexual displays is linked to personality and results in reproductive performance trade‐offs for male A. studiosus.     

The relationship between female urinary estrogen excretion and mating behavior in cotton-topped tamarins,Saguinus oedipus oedipus

Daily urinary estrogen excretion in six singly housed adult female cottontopped tamarins was measured by radioimmunoassay. Each female was paired with a male for 1 hr every day, during which behavioral observations were conducted on the pair from behind a oneway glass screen. During each observation period the duration or frequency of occurrence of various behaviors was recorded. In this paper, the daily variations of (1) total frequency of male mounting, (2) total frequency of male mounting with thrusting, and (3) latency to first male mount are presented in relation to the measured pattern of female estrogen excretion. The results reveal a high degree of behavioral variation between pairs, although a relationship between rhythmic changes in sexual activity and female estrogen excretion in individual pairs is apparent. Mating occurs throughout the female cycle and also during at least the first 2–3 weeks of pregnancy. A gestation period of 170–172 days is estimated in respect of one female, in agreement with a previous observation of one gestation of at least 166 days. The high frequency and intensity of mating recorded in this controlledintroduction study give support to the proposition that mating is important in pairbonding in this monogamous species. It is concluded that under the experimental procedure followed, mating behavior did not reliably reflect the female’s reproductive hormonal state.     

Mating behaviors of the proboscis monkey (Nasalis larvatus)

The mating behaviors of the proboscis monkey were observed in a riverine forest along a tributary of the Kinabatangan River, Sabah, Malaysia, for a period of 30 months. Solicitation for copulation was initiated frequently by males and occasionally by females. Most copulations involved only one mount; however, some multiple-mount copulations were observed and a maximum of six mounts per copulation were recorded. The mean duration of mounts was about 27 sec. Nonsexual mounts (female-female, female-juvenile/infant, juvenile-juvenile, and juvenile-infant) were also observed. Female-female mounts occurred shortly after failed solicitations toward males were observed. Harassment by juveniles and/or infants was observed during copulation; however, these harassments apparently did not interfere with copulation. Sexual swelling was evident in 77.4% of copulating females, with copulating subadult females showing the most distinct swelling.     

Affiliative interference in mounts in a group of Tonkean macaques (Macaca tonkeana)

Affiliative interference in mounts was studied in a group of Tonkean macaques (Macaca tonkeana) living in semi-liberty. Over a 4-year period, 545 sexual and noncopulatory mounts accompanied by 367 instances of interference were recorded using behavior-dependent sampling. Interference by immature individuals was frequent and occurred mainly when the mother was the mountee. Interference by adult females was less common. Various behavior patterns were displayed in interference, mainly directed toward the mounter. Aggression by the latter was rare. However, interference occurred from further away with increasing age of the interfering individual. It is suggested that interference represents an attempt to be involved in interactions with influential individuals. Comparisons with other species support the hypothesis that the development of interference is related to species-typical social relationships and, in particular, that frequency and intensity of interference are determined by the tolerance of adult males.     

Male Post‐Ejaculatory Mounting in the Ring‐Tailed Lemur (Lemur catta): A Behavior Solicited by Females?

Male mate guarding can take many forms but often involves aggression toward male conspecifics and continued proximity with a female. This study describes a previously undocumented behavior in a promiscuous primate, the ring‐tailed lemur: post‐ejaculatory (PE) mounting. PE mounting was documented across eight mating seasons in a ring‐tailed lemur colony on St. Catherines Island (SCI), USA. During PE mounting, a male remounts a female following ejaculation and clasps her midsection as if to mate again, but copulation does not occur; males showing this behavior typically lack erections, and their mounts show an absence of penile intromission and rhythmic thrusting. Male PE mounting was more common among males mating earlier in the queue, and when PE mounting occurred, it accompanied mate guarding. Four non‐mutually exclusive hypotheses to explain PE mounting were evaluated as follows: (1) gaining additional copulations, (2) prevention of re‐mating, (3) lengthening sperm residence time, and (4) re‐mounting as a function of female proceptivity. Male PE mounting did not aid males in gaining additional copulations nor did PE mounting prevent females from mating with new males. Equivocal support was found for Hypothesis 3: although there was much overlap in copulatory plug residence times for males who did and did not show PE mounting, one‐third of males who practiced PE mounting had plug residence times of 2 h or more, much longer than that of males who did not show PE mounting. PE mounting may therefore be related to increased plug residence time, which may provide an advantage to males in sperm competition. Strong evidence was found in support of Hypothesis 4: males overwhelmingly performed PE mounts in response to continued female sexual presentations, suggesting that females can solicit this male behavior. Females consequently exercise an even greater degree of control over males than was previously realized in this ‘female dominant’ primate.