Reproduction in wild female olive baboons

The purpose of this paper is to evaluate several factors that influence female reproduction in a large troop of wild olive baboons (Papio cynocephalus anubis) based on 4 consecutive years of demographic data. Interbirth intervals were significantly shorter for females whose infants died before their next conception than for females whose infants survived. High-ranking mothers of surviving infants had significantly shorter birth intervals than comparable low-ranking mothers, independent of maternal age. This occurred mainly because the interval from resumption of cycling to conception was significantly shorter for high-vs. low-ranking females. Dominance rank did not influence sex ratio at birth, infant survival in the first 2 years, or adult female mortality. Age was also significantly related to interbirth intervals, with older females having shorter intervals. Primiparous females had consistently longer reproductive intervals than did multiparous females, but this difference reached statistical significance only for females whose infants died before the next conception. Primiparous females also experienced significantly higher infant mortality. Data on body size and estrous cycle length indicated no differences between high- and low-ranking females. Nutritional and stress-related mechanisms that may underlie the reproductive advantages of high rank are discussed.     

Birth spacing in langur monkeys (Presbytis entellus)

This paper presents 10 years of reproductive data on birth interval length and 5 years of data on reproductive behavior postpartum from a captive colony of gray langur monkeys (Presbytis entellus)housed in Berkeley, California. Birth intervals of females following different pregnancy and nursing schedules are compared. Females whose infants survive to the age of 9 months have a median birth interval of 15.4 months. The experimental separation of mothers from infants for a period of 2 weeks, 6 to 9 months postpartum, had no significant effect on the median birth interval length. Females experiencing a pregnancy failure or the loss of a neonate had median birth intervals of 9.6 and 10.7 months, respectively. These intervals were significantly shorter than the birth intervals of females whose infants survived to 9 months, showing that the presence of a nursing infant delays the female’s time to next conception by approximately 5 to 6 months. Females experienced a median of three estrous periods (two estrous cycles) before conceiving postpartum, regardless of pregnancy outcome or length of infant survival, and females rarely conceived during their first estrous period postpartum. Weaning did not occur until after the mother’s next conception. These data indicate that, in populations of langurs characterized by average birth intervals of 15 to 16 months, the loss of an infant after the age of 5 to 6 months will not accelerate a female’s ability to conceive or shorten the birth interval length. The available data on birth spacing from populations of free-ranging langurs are reviewed. It could not be demonstrated that non-Himalayan populations are characterized by birth intervals which are as long as 20 to 24 months. Rather, it is suggested that female langurs inhabiting seasonally arid sites, such as Jodhpur, Abu, and Dharwar, may be capable of producing infants on the average of every 15 to 16 months. Flexibility in the timing of births and the lack of well-defined birth seasons at these sites may be explained by this species’ dietary and digestive adaptations. Additionally, data on birth spacing and the age of missing infants from the above field sites, where it has been suggested that infanticide following changes in male leadership occurs habitually, do not lend support to the sexual selection hypothesis of infanticide as proposed by S. Hrdy (1974, 1977).     

Life history of hamadryas baboons: Physical development,infant mortality,reproductive parameters and family relationships

Demographic and life history parameters were estimated for a band of free-ranging hamadryas baboons, observed for 5.5 years in Ethiopia. Age-related changes in body weight and dentition were found to be delayed relative to laboratory-reared baboons. On the average, females reached menarche at 4.3 years of age and had their first infant at the age of 6.1 years. The mean interbirth interval was 24 months if the infant survived this period. The survival of infants and juveniles was higher compared to Amboseli yellow baboons, but somewhat lower than in gelada baboons in the Simen Mountains. Males acquired their first juvenile or adult female at the age of 8.5 to 11 years. Male-female pair-bonds lasted several years in most cases. The Cone Rock baboons were organized in a four-level social structure. The troop could split into bands, bands were divided into clans, and clans into one-male units with bachelor followers. The exchange of individuals between social units predominantly occurred within the band. All males of known origin became adult members of their presumed natal clan. Most females transferred also within clans, and juvenile females tended to remain in their natal clan. Females lost by one male to several rivals tended to reassemble in the same new one-male units later on.     

Birth dynamics in Hanuman langurs,Presbytis entellus of Jodhpur,India

Ten years data on birth peak, birth rate and interbiith interval inPresbytis entellus of Jodhpur have been presented. Although Hangman langur females breed round the year, there is some concentration of births during January–March while fewer births occur during October–December. It seems that provisioning and crop raiding together may provide better feeding opportunities to breed year round. However, it remains unclear whether environmental factors allow langur females to deliver more infants during January–March. During 1984–86 the birth rate was uniform for the whole population (0.63). While there was a variation within the troops from year to year, data suggest that resident male replacements do alter birth rate. It goes down when resident males are replaced frequently. The interbirth interval ranges between 7.0 and 76.5 months (average, 16.88 months;n = 112). Abortions and still-births reduced the interbirlh interval to 7.1 months (range 7.1-21.1; average, 11.4 months;n= 8) compared to the normal inlerbirth interval following infant survive its first 4.1 months of life (range 10.7-76.5 months; average, 17.28 months;n = 86). However, infant loss under the age of 4.1 months did not reduce the interbirth interval except in two cases (range 7.0-51.8 months; average, 17.27 months;n = 18). Maternal rejection or weaning begins at about 8 months of age and lasts until infants are 12 months old. In this population, the probability of twin births was worked out to be 0.79 per 100 births.     

Female Reproductive Parameters of Tana River Yellow Baboons

We describe the female reproductive parameters of yellow baboons at the Tana River National Primate Reserve, Kenya. We present data on menarche, cycle length, pregnancy, birth, postpartum amenorrhea, interbirth interval, and infant survival. We also briefly compare our data to those reported for yellow baboon females at the Amboseli Reserve, Kenya. Our results indicate statistically significant differences in some of these reproductive parameters between the two sites.     

Troop history,female reproductive strategies and timing of male change in Hanuman langurs,Presbytis entellus

Female reproductive data are presented from 9 years of longitudinal observations on two troops of Hanuman langurs (Presbytis entellus) living around Jodhpur, India. On the basis of 89 live births interbirth intervals were calculated to examine the effect of demographic factors on reproductive behaviour and troop composition. Sex of an infant seems to influence the length of intervals which are longer after the birth of female infants at an average of 1.7 months. It is suggested that this may be an outcome of differential maternal investment by allocating more time and energy towards female infants who run a higher mortality risk than male infants, at least up to an age of 27 months. Troopspecific interbirth intervals are influenced by social events. If the last infant is still alive when the next one is conceived, the intervals are significantly longer than after the premature loss of an infant (Bijolai troop: 15.6 vs. 12.1 months; Kailana-1 troop: 16.7 vs. 11.4 months). During undisturbed male tenureship intervals are shorter than after a male change (Bijolai troop: 14.3 vs. 16.0 months; Kailana-I troop: 15.6 vs. 17.5 months). Thus the frequency of male changes can influence the demography of a troop. Furthermore, the data suggest that take-overs are optimally timed by males. New males tend to take over a troop when most of the females are cycling.     

Female weight and reproductive condition in a population of olive baboons (Papio anubis)

The study reported here tested Altmann's prediction [Baboon Mothers and Infants. Cambridge, Harvard University Press, 1980] that lactating female baboons endure a weight loss. Data from 64 adult female olive baboons (Papio anubis) residing in six troops in Kenya revealed that reproductive condition was related to weight. Lactating females weighed less and pregnant females weighed more than cycling females. There was a negative correlation between the weight of cycling females and the number of months postweighing to their next conception. These results indicate that lactation in wild baboons imposes energy costs that result in lost weight. It is suggested that female baboons may have to surpass a minimum weight threshold prior to resumption of postlactational cycling and that nutritional status is more influential than rank in affecting female reproductive success.     

Demography of Amboseli baboons, 1963–1983

Repeated censuses of a population of yellow baboons (Papio cynocephalus) in Amboseli National Park, Kenya, revealed a decrease from over 2,500 animals in 1963–1964 to 123 individuals in 1979, or from a density of about 73 to 1.8 baboons per km² over a 15-year period. Median group size decreased from 43 in 1964 to 27 in 1979. The largest and smallest groups declined the most; groups near the median have maintained fairly stable size and age distributions. The population seemed to have stabilized by 1983 at approximately 150 animals in six groups (median group size 28; density 2.2/km²). Although baboon population and group size appeared to be stable during 1963–1964, the age distribution and demographic parameters (age-specific mortality and natality for one social group) during that year indicate that the population decline had already started. The rate of population decline was greatest in the 1964–1969 period and remained appreciable during the next 5 years. The decline of the baboon population was paralleled by that of other Amboseli savannah woodland mammalian species and took place during a period of very high mortality of fever trees (Acacia xanthophloea) and extensive invasion of the area by halophytes, a transition brought on by rising ground water and consequent elevation of the soil salinity zone. In this and several other primate populations, mortality of infants and juveniles appears to be the demographic variable most sensitive to environmental change.     

Physical maturation and age estimates of yellow baboons,Papio cynocephalus,in Amboseli National Park,Kenya

In a longitudinal study of individually identified wild baboons in Amboseli National Park, Kenya, we collected data on physical development and reproductive maturation. Confirming and extending our earlier results, we demonstrated that the ratio of ages at which developmental milestones occur in the field as compared to those under extensive provisioning or in captivity were approximately 5:3. The age range for some developmental milestones was quite narrow and discrete, while for others there was considerable between-individual variability and more gradual changes. For infants, only the change from pink to gray of the paracallosal skin occurred within a brief age span. For older animals two important developmental events are readily identified and occur within a fairly narrow age range: Rapid enlargement of testes at 5 to 6 years for males and onset of menarche at 4 to 5 ½ years for females. In the present report, we considered some consequences of accelerated or delayed maturation. We further explored the need to employ different age-class criteria for different research problems.     

Effects of age,rearing, and separation stress on immunoglobulin levels in rhesus monkeys

The study reported here examined the effect of different rearing conditions and psychological stress on immunoglobulin levels in rhesus monkey infants. In the first experiment, 24 rhesus neonates were placed in one of the three following rearing conditions: Separated from their mothers and reared in the laboratory nursery; kept with their biological mothers; or removed at birth from their biological mothers and cross-fostered to adoptive rhesus mothers. Plasma samples were obtained from the nursery-reared infants immediately after birth and at weekly intervals for the next 30 days. Samples were also obtained from mother-reared and foster-reared infants on days 15 and 29. All samples were tested for IgG and IgM levels. The results indicated that neither rearing nor diet affected Ig levels. IgG levels were highest at birth and decreased progressively for the first 30 days, suggesting that placental transfer of maternal IgG is the critical determinant of IgG levels in primate infants as in humans. IgM changes were also similar to those in human infants: Low levels at birth, a significant increase from birth to day 15, and a moderate decline from day 15 to day 30. When IgG levels and IgM levels were correlated across the first month, many significant correlations were found which were consistent with human data relating both infant IgG and IgM levels to infant maturation. In the second experiment, 11 of the previously tested nursery infants were subjected to four consecutive social separations from peer groups at 6 months of age. Plasma samples were obtained before and after the first and fourth weeks of separation and tested for IgG and IgM levels. Small but significant decreases in both immunoglobulins were detected after 4 days of separation, particularly on the fourth week.     

Double infanticide in a free-ranging group of buffy-headed marmosets, Callithrix flaviceps

This study describes two infanticides in a free-ranging group of Callithrix flaviceps. In November 2008, four females gave birth within a period of approximately 10 days. On the day after the third birth, the new mother was attacked by an unidentified individual, resulting in the death of one of her infants due to a bite to the top of the head. Five days later, the fourth female gave birth to twins, and the next day, the more socially dominant of the breeding females was observed ingesting the head of one of these infants. All other infants survived until the end of the study. With the exception of the unusual number of births and attacks, the behaviour appeared typical of that recorded in other marmosets, where socially dominant breeding females attack the offspring of subordinates, apparently as a strategy aimed at reducing competition for the services of infant caregivers.     

Social relations in a free-ranging troop of stumptail macaques (Macaca arctoides): Male-care behaviour I

The occurrence of male-care behaviour directed from juvenile and adult males to infants was studied in a free-ranging troop of Stumptail macaques. The study period lasted two months comprising about 140 hours of recorded observations. Infants were a focal subgroup and their interactions with older males were recorded. The following variables were examined in relationship to the sending and receiving of male-care: the infant (its age, sex, and dominance rank), older males (their age and dominance rank), and genetic ties. Infants I received more male-care than infants II and differences in the type of male-care received by infants I and II were found. Male infants received more male-care than female infants and sex differences in the type of care received were evident. No relationship was found between the infant’s dominance rank and the amount of male-care received. A substantial amount of male-care behaviour was sent to genetic kin. Two-three year olds displayed more male care than yearlings. Juveniles as a class displayed more male-care than adults. A positive association was found between the juveniles’ dominance rank and the sending of male-care. However, among the adults, the subordinate male displayed more care behaviour than the alpha male. The presence or absence of the mother was found to influence the older males’ interest in the infant. The results are discussed and compared with data available on other primate species. Supported by grants from the Behavioral Science Foundation (U.S.) and by the Mexican Institute of Anthropology.     

Some developmental markers in yellow baboon infants of Mikumi National Park,Tanzania

Infants of known birthdates were sampled from a population of yellow baboons (Papio cynocephalus) in Mikumi National Park, Tanzania, to ascertain the reliability of several maturational changes which could be used to age infants whose birthdates are unknown. The transition from the infant's black natal coat to the uniform yellow or tan adult pelage proved extremely variable, with completion varying from 7 to 19 months. The transition from the pink skin of the newborn to the completely grey adult pigmentation was much less variable. Skin on the hands and feet and on the paracallosal area was completely grey in all individuals by 8 months, while skin on the face and ears changed more gradually and was entirely grey by 12 months. These data are in substantial agreement with maturational markers established for yellow baboon infants in Amboseli National Park, Kenya, despite differences in habitat and age-sex structure between the two populations.     

Thermal effects on movement patterns of yellow baboons

This paper examines the effect of thermal environment on movement patterns of free-ranging yellow baboons (Papio cynocephalus). For Amboseli baboons, one source of potential thermal stress is intense midday heat, and a plausible thermoregulatory response is for animals to simply move into the shade. I therefore examined the hypothesis that baboons would choose quadrats with higher shade availability (as measured by vegetation cover) in response to increasing midday heat loads (as measured by air temperature and solar radiation). Surprisingly, this was not the case—neither ambient air temperature, ambient solar radiation, nor quadrat plant species composition had a significant effect on shade availability of quadrat selected. Instead, thermal conditions affected a different aspect of baboon movements; namely, spatial displacement rates. At high air temperatures, baboons as a group traversed woodland habitats more slowly, and bare pans more quickly, than at lower air temperatures. I surmised that this relationship might reflect thermal effects on movement patterns at a smaller scale: if individuals exposed to high heat loads spent more time resting in shade under clumps of vegetation, they would thereby traverse densely-vegetated (hence shaded) quadrats more slowly. To address this question directly, I obtained focal sample data on activity and microhabitat budgets of individual baboons in relation to environmental temperature. The frequency of most combinations of activity state (e.g., grooming, social behavior) and microenvironment state (e.g., elevation, proximity to vegetation) did not vary monotonically with air temperature. However, baboons in shaded locations (but not those in unshaded locations) spent more time resting and less time moving at high air temperatures than low. In other words, baboon activity budgets depended on both microclimate and microhabitat—animals reduced their activity, particularly movement, when they encountered shade under hot conditions. This pattern of microhabitat choice in turn led to temperature-dependent changes in travel rate at the habitat level. These observational studies of movement patterns suggest that Amboseli baboons employ opportunistic thermoregulation—they do not seek out densely-shaded habitats or individual patches of shade at high air temperatures. Instead, they respond to environmental heat loads by resting, and thereby slowing down, when they happen to encounter plant shade. Aspects of baboon ecology that favor such an opportunistic mode of thermoregulation include large body size and non-thermal constraints on movement patterns.     

Vervet monkey grandmothers: Interactions with infant grandoffspring

Social relationships of 30 infants with their maternal grandmothers were studied in a captive colony of vervet monkeys (Cercopithecus aethiops sabaeus).Grandmothers and grandinfants formed affiliative relationships with one another that could be distinguished from the infant’s relationships with nonkin adult females and with other adult female kin. The intensity of the grandmother—grandinfant relationship varied according to several factors which were related to the infant’s vulnerability to mortality and to the grandmother’s ability to provide effective social support. High-ranking grandmothers spent more time near their grandinfants, and initiated more grooming and caretaking of their grandinfants, than did lower-ranking grandmothers. Grandmothers spent more time near their daughter’s first surviving infant than near later-born infants, and when grandmothers had more than one adult daughter, they spent more time near the infant of the younger daughter. These results, combined with the fact that the presence of a maternal grandmother has been associated with a reduction in the rate of infant mortality in this colony (Fairbanks and McGuire, 1986), suggest that grandmothers are actively contributing to the reproductive success of their adult daughters and to the survival of their infant grandoffspring.     

Dominance and reproductive rates in captive female olive baboons, Papio anubis

The reproductive cycles of 23 captive olive baboons were studied over two successive parturitions. Interbirth intervals of 450 days were reduced by 60% in comparison to wild baboons, and consisted of 145 days of postpartum amenorrhea, 3.5 cycles, and a gestation of 185 days. Dominance rank was found to be one significant factor affecting female fertility. Low-ranking females had longer total intervals between successive births and, in particular, they experienced a longer delay to conception once they had resumed sexual cycles. Mothers of infants who were heavy for age resumed cycling more quickly and had fewer cycles before a subsequent conception. Mothers best able to sustain rapid early infant growth were those of high dominance rank and of high body mass; these females had more rapid reproductive rates. As female energy intake was unrelated to dominance, we suggest that social stresses are important suppressors of the hormonal and lactational competence of subordinate females.     

Persistence of maternal effects in baboons: Mother's dominance rank at son's conception predicts stress hormone levels in subadult males

Dominance status and reproductive experience are maternal characteristics that affect offspring traits in diverse taxa, including some cercopithecine primates. Maternal effects of this sort are widespread and are sources of variability in offspring fitness. We tested the hypothesis that maternal dominance rank and reproductive experience as well as a male's own age and dominance rank predicted chronic fecal glucocorticoid (fGC) concentrations in 17 subadult wild male baboons, Papio cynocephalus (median age 6.5 years), in the Amboseli basin, Kenya. Among these variables, maternal dominance rank at a subadult male's conception was the sole significant predictor of the male's fGC and accounted for 42% of fGC variance; sons of lower ranking mothers had higher fGC than did those of high-ranking mothers. This result is striking because subadult male baboons are approximately 4-6 years past the period of infant dependence on their mothers, and are larger than and dominant to all adult females. In addition, many males of this age have survived their mothers' death. Consequently, the influence of maternal dominance rank persisted well beyond the stage at which direct maternal influence on sons is likely. Persistence of these major maternal influences from the perinatal period may signal organizational effects of mothers on sons' HPA axis. Although short-term, acute, elevations in GC are part of adaptive responses to challenges such as predators and other emergencies, chronically elevated GC are often associated with stress-related pathologies and, thereby, adverse effects on fitness components.     

Chimpanzee triplets born in captivity

A female chimpanzee (Pan troglodytes) gave birth to triplets at the Lincoln Park Zoological Gardens, Chicago, Illinois. Of the three infants born, only one survived. The other two, both sexed as males, were dead when they were discovered. When pathology was done on these infants, it was found that aside from being underweight, chimpanzee No. 1 was 930 g and chimpanzee No. 2, 630 g, the animals had never developed a brain. The female nursed the surviving male infant for six days till it was taken for hand-rearing. The infant was in a weakened condition and weighed 890 g. He died on the next day. This is possibly the first birth of triplet chimpanzees in a North American zoological garden.     

Low birth weight, maternal birth-spacing decisions, and future reproduction

The aim of this study is an analysis of the possible adaptive consequences of delivery of low birth weight infants. We attempt to reveal the cost and benefit components of bearing small children, estimate the chance of the infants’ survival, and calculate the mothers’ reproductive success. According to life-history theory, under certain circumstances mothers can enhance their lifetime fitness by lowering the rate of investment in an infant and/or enhancing the rate of subsequent births. We assume that living in a risky environment and giving birth to a small infant may involve a shift from qualitative to quantitative production of offspring. Given high infant mortality rates, parents will have a reproductive interest in producing a relatively large number of children with a smaller amount of prenatal investment. This hypothesis was tested among 650 Gypsy and 717 non-Gypsy Hungarian mothers. Our study has revealed that 23.8% of the Gypsy mothers had low birth weight (<2,500 g) children, whose mortality rate is very high. These mothers also had more spontaneous abortions and stillbirths than those with normal weight children. As a possible response to these reproductive failures, they shortened birth spacing, gaining 2–4 years across their reproductive lifespan for having additional children. Because of the relatively short interbirth intervals, by the end of their fertility period, Gypsy mothers with one or two low birth weight infants have significantly more children than their ethnic Hungarian counterparts. They appear to compensate for handicaps associated with low birth weights by having a larger number of closely spaced children following the birth of one or more infants with a reduced probability of survival. The possible alternative explanations are discussed, and the long-term reproductive benefits are estimated for both ethnic groups.