Reproduction and social rank in female stumptail Macaques (Macaca arctoides)

Reproductive physiology was studied in female stumptail macaques. Initially the monkeys were housed indoors (individually and in small groups) and later as one large (92 individuals) social group in an outdoor cage. Most data were collected during the 4-year outdoor period. Plasma progesterone determination in blood samples taken at weekly intervals allowed estimation of ovulation and conception dates. The age at first ovulation (X =3.73 years) was positively correlated with body weight at 3 years of age. The average age at first birth was 4.90 years. Gestation lengths averaged 176.6 days. Following a live birth ovulations returned after a mean interval of 11 months but following an abortion or still birth this interval was 1 month. Usually a number of ovulatory cycles (X =2.37) preceded a conception. Interbirth intervals (IBIs) in the outdoor cage (X =619.4 days) were significantly longer than IBIs during the indoor period (X =523.1), because indoors the infants were weaned at the age of 7 months, while outdoors weaning occurred more naturally. IBIs following abortions or still births (X =291.9 days) were significantly shorter than IBIs following live births. Age at first ovulation, age at first birth, IBIs, and infant production rates were not correlated with dominance rank. Ovarian cycle lengths (X =30.2 days, mode = 28 days) were comparable to previously reported data from laboratory-housed stumptails. No systematic seasonal fluctuations were found in the onset of sexual maturity, in ovarian cycle lengths, in copulation frequencies, and in distribution of births.     

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.     

SEASON OF BIRTH AND REPRODUCTIVE PERFORMANCE: AN ANALYSIS OF FAMILY RECONSTITUTIONS OF 800 WOMEN BORN IN THE NETHERLANDS AT THE END OF THE 19TH CENTURY

Background: Several studies have reported associations between season of birth and reproductive characteristics such as menarcheal age, fecundability, and twinning, but the results are inconsistent with respect to the location of high- and low-risk seasons. To assess whether this disagreement could be due to the use of populations from different geographic areas and time frames instead of different etiologic pathways, we investigated the season-of-birth dependency of a variety of reproductive outcomes within one time- and arealimited population. Methods: In a historic follow-up study, the reconstituted families of 800 women born between 1873 and 1887 in or near Rotterdam, The Netherlands, were used to determine eight types of reproductive outcome: childlessness, interval to first pregnancy, pregnancy interval, stillbirth, neonatal death, postneonatal death, multiple birth, and gender of offspring. The relation of these outcomes with season of birth was modeled using cosinor functions with periods of 1 year or a half year. Data were analyzed by use of logistic regression or general estimation equations (GEE), dependent on whether outcomes could occur more than once per woman. Results: Peaks in the model-based risks of reproductive failure were found within two small temporal ranges, January 1 to February 11 and July 1 to August 11 for all outcomes except gender. The picture did not change after controlling for known and possible risk factors, including age, offspring's birth cohort, and some social variables. Conclusions: This study reconfirms the idea that seasonal factors around conception or birth influence later reproductive characteristics. Observing the consistency of the location of high-risk seasons across a variety of outcomes, the explanation of season-of-birth dependency of different reproductive outcomes need not involve multiple etiological pathways. (Chronobiology International, 18(3), 525–539, 2001)     

Associations of Aging and Birth Cohort with Body Mass Index in a Biethnic Cohort

Objective: To examine associations of aging and birth cohort with body mass index (BMI) in a biethnic cohort. Research Methods and Procedures: This was a longitudinal closed cohort study of 14, 500 white and African‐American men and women, 45 to 64 years of age, followed for 9 years. Aging was defined as the length of the interval in years between baseline and following visits. Birth cohort was defined by the year in which participants were born. Mixed model analyses were used to examine associations of aging, birth cohort, and BMI in four ethnicity‐gender groups. Results: We found that aging was associated with an increase in BMI in white and African‐American men and women. The associations between aging and BMI were stronger in the younger birth cohorts. Except for white women, younger birth cohort was associated with a higher BMI. After adjusting for aging, birth cohort was associated with an increase in BMI of 0.1 kg/m² [95% confidence interval (95% CI): ?0.1, 0.3] among white women. The corresponding values for African‐American women, white men, and African‐American men are 0.5 kg/m² (95% CI: 0.1, 0.9), 0.6 kg/m² (95% CI: 0.4, 0.8), and 0.6 kg/m² (95% CI: 0.2, 1.0), respectively. Discussion: Our analyses show that, in all except white women, people in this age range who were born later have a higher BMI at the same attained age. In all groups, people who are born later gained more weight as they aged. In general, subjects ages 45 to 64 years gained weight as they aged 9 years.     

Reproductive Strategies of <Emphasis Type="Italic">Trachypithecus pileatus</Emphasis> in Arunachal Pradesh,India

We studied reproductive behavior of free-ranging capped langurs (Trachypithecus pileatus) in the Pakhui Wildlife Sanctuary, Arunachal Pradesh, India. Four species of primates —Trachypithecus pileatus, Macaca mulatta, M. assamensis, and Nycticebus bengalensis— live there. We studied the mating seasons, mating frequency, copulatory attempts, time spent in copulation, and interval between 2 successive copulations, gestation length, and interbirth interval of 4 groups of capped langurs during 2001–2003. We observed 2 mating seasons in a year. The first was larger, comprising 5 months (September–January), and the second was short, April and May. Mating was intensive in the morning session (0600–1000 h); 57% of total mating events occurred then. The average gestation period was 200 d. November was the most favorable month for breeding. In a year, 107 mating events occurred involving 5 adult females. Average time per mounting attempt is 12 s. Duration of mounting was the maximum in November. Interbirth interval was 23 months and 10 d. The birth season was 129 days, December–April; 53% of births occurred in February and March. Average birth rate is 0.386 birth/female/yr.     

Association between Birth Interval and Cardiovascular Outcomes at 30 Years of Age: A Prospective Cohort Study from Brazil

Background

Birth interval is an important and potentially modifiable factor that is associated with child health. Whether an association exists with longer-term outcomes in adults is less well known.

Methods

Using the 1982 Pelotas (Brazil) Birth Cohort Study, the association of birth interval with markers of cardiovascular health at 30 years of age was examined. Multivariable linear regression was used with birth interval as a continuous variable and categorical variable, and effect modification by gender was explored.

Results

Birth interval and cardiovascular data were present for 2,239 individuals. With birth interval as a continuous variable, no association was found but stratification by gender tended to show stronger associations for girls. When compared to birth intervals of <18 months, as binary variable, longer intervals were associated with increases in height (1.6 cm; 95% CI: 0.5, 2.8) and lean mass (1.7 kg; 95% CI: 0.2, 3.2). No difference was seen with other cardiovascular outcomes.

Conclusions

An association was generally not found between birth interval and cardiovascular outcomes at 30 years of age, though some evidence existed for differences between males and females and for an association with height and lean mass for birth intervals of 18 months and longer.     

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).     

A note on the dispersionless growth law for single cells

A population of initially synchronized cells is considered wherein each cell grows according to a dispersionless growth law and the probability of cell division is determined by cell age. The first and second moments of the distribution of birth volumes are considered as functions of time and it is shown that it is impossible for both moments to approach finite, nonzero limits ast→∞. This implies that the volume distribution of the population will not approach a limiting distribution on any finite, nonzero volume interval and that the population will not attain balanced exponential growth. An illustrative example is worked out in detail. The distribution of birth volumes is also analyzed as a function of generation number and it is found that the logarithm of the birth volume in thejth generation is normally distributed asj→∞, with an unbounded variance. Generalizations and implications of these results are briefly discussed. Work supported by the U.S. Atomic Energy Commission.     

Estimating population birth rates of zooplankton when rates of egg deposition and hatching are periodic

Summary I present a general method of computing finite birth and death rates of natural zooplankton populations from changes in the age distribution of eggs and changes in population size. The method is applicable to cases in which eggs hatch periodically owing to variable rates of oviposition. When morphological criteria are used to determine the age distribution of eggs at the beginning and end of a sampling interval, egg mortality can be incorporated in estimates of population birth rate. I raised laboratory populations of Asplanchna priodonta, a common planktonic rotifer, in semicontinuous culture to evaluate my method of computing finite birth rate. The Asplanchna population became synchronized to a daily addition of food but grew by the same amount each day once steady state was achieved. The steady-state rate of growth, which can be computed from the volume-specific dilution rate of the culture, was consistent with the finite birth rate predicted from the population's egg ratio and egg age distribution.     

Reproductive parameters of wild Trachypithecus leucocephalus: seasonality,infant mortality and interbirth interval

Understanding the reproductive parameters of endangered primate species is vital for evaluating the status of populations and developing adequate conservation measures. This study provides the first detailed analysis of the reproductive parameters of wild white‐headed langurs (Trachypithecus leucocephalus), based on demographic data collected over an 8‐year period in the Nongguan Karst Hills in Chongzuo County, Guangxi, China. From 1998 to 2002, a total of 133 live births were recorded in the population based on systematic censuses. Births occurred throughout the year, but the temporal pattern was highly correlated with seasonal variation in temperature and rainfall, with the birth peak coinciding with the dry and cold months of November–March. The average birthrate was 0.47±0.13 births per female per year and mortality for infants younger than 20 months was 15.8%. From 1998 to 2006, 14 females gave birth to 41 infants in four focal groups. The average age at first birth for female langurs was 5–6 years (n=5) and the interbirth interval (IBI) was 23.2±5.2 months (median=24.5 months, n=27). Infants are weaned at 19–21 months of age. The IBI for females with infant loss before weaning was significantly shorter than those for females whose infants survived. It appears that birth seasonality in the white‐headed langurs is influenced by seasonal changes in food availability. The timing of conceptions was found to coincide with peak food availability. The reproductive parameters for white‐headed langurs reported here are quite similar to those reported for other colobine species. One major difference is our observation of lower infant mortality in Trachypithecus. Am. J. Primatol. 71:558–566, 2009. © 2009 Wiley‐Liss, Inc.     

Birth in winter can reduce the risk of lung cancer: A retrospective study of the birth season of patients with lung cancer in Beijing area,China

The season of birth is an important risk factor for several diseases. We explored the relationship between birth season and lung cancer. In this population-based retrospective study, we focused on patients with lung cancer who had registered at the Beijing Institute for Cancer Research from 2003 to 2012. In total, 33,025 patients were divided into five subgroups based on their histologic classification, and these five subgroups were compared with the general population (i.e., the permanent resident population of Beijing in 2013). A binary logistic regression method with sex and age as control factors was used to evaluate the relationship between birth season and lung cancer; P < 0.01 was statistically significant. Taking winter as a reference in our analysis of the relationship between season of birth and lung cancer, we found that people who were born in other seasons had a higher probability of developing lung cancer (spring: odds ratio [OR] = 1.06, 95% confidence interval [CI] = 1.03–1.09; summer: OR = 1.07, 95% CI = 1.04–1.10; autumn: OR = 1.06, 95% CI = 1.03–1.09) (P < 0.01). Among the five subgroups, persons with squamous cell carcinoma who were born in summer were more likely to develop lung cancer than those who were born in winter (OR = 1.09, 95% CI = 1.02–1.15, P = 0.006). The other subgroups showed no correlation with season of birth (P > 0.01). This study demonstrates that for people born in winter, the risks of developing lung cancer and squamous cell carcinoma are comparatively lower than those for people born in other seasons. Differences in immune function and the maternal nutrition status during pregnancy of people born in different seasons may explain this finding.     

Control of postpartum mating behavior in free-ranging rhesus monkeys

This paper explores the effect that a dependent rhesus macaque infant (Macaca mulatta) has on the timing of its mother's resumption of mating. Toward this end, behavioral data from the rhesus populations at Tughlaqabad, India, and Cayo Santiago, Puerto Rico, are compared. Specifically, the intervals between parturition and subsequent resumption of mating for individual parous females are examined in order to shed light on the relative importance of environmental and internal factors (such as lactational infertility) in the control of rhesus mating behvior. At both study sites it was found that the later a given female gave birth during a birth season the shorter was her parturition-mating interval and the younger was her infant when she resumed mating activity. It is suggested that this finding is the result of an interaction of environmental and internal factors; both act in concert to determine how soon after parturition a particular rhesus female will resume mating activity.     

Effect of delivery season on subsequent birth interval in early 20th century in Japan

Questionnaires of birth dates of family members (13 404 families in total) were analyzed in order to examine the effects of delivery season of a baby on the subsequent birth interval. Deliveries at maternal age of 20–34 years were used. In 1921–1935, the mothers who had been delivered of a baby in August–October showed the shortest (30.62 months geometric mean) and those in February–April the longest (34.05 months) non-last intervals, with a highly significant difference among the four delivery seasons (P<0.001, Kruskal-Wallis test,n=5678). Although the intervals were abruptly prolonged just before the last birth, the above difference was also consistent in the last intervals. When seasonal distributions of last and non-last births were compared, last births tended to be concentrated in the summer half of a year (P<0.05) in 1921–1935. In 1951–1965, overall geometric mean of the interval shortened to 28.44 months, and the length of intervals did not differ appreciably according to the season of preceding delivery. Deliveries in late summer (August–October) in 1921–1935, therefore, were associated with increased risk of termination of reproduction, on one hand, but a lowered chance of prolongation of the subsequent interval, on the other hand. Possible environmental factors are discussed to explain this apparently paradoxical phenomenon.     

Effects of inbreeding on fitness‐related traits in a small isolated moose population

Inbreeding can affect fitness‐related traits at different life history stages and may interact with environmental variation to induce even larger effects. We used genetic parentage assignment based on 22 microsatellite loci to determine a 25 year long pedigree for a newly established island population of moose with 20–40 reproducing individuals annually. We used the pedigree to calculate individual inbreeding coefficients and examined for effects of individual inbreeding (f) and heterozygosity on fitness‐related traits. We found negative effects of f on birth date, calf body mass and twinning rate. The relationship between f and calf body mass and twinning rate were found to be separate but weaker after accounting for birth date. We found no support for an inbreeding effect on the age‐specific lifetime reproductive success of females. The influence of f on birth date was related to climatic conditions during the spring prior to birth, indicating that calves with a low f were born earlier after a cold spring than calves with high f. In years with a warm spring, calf f did not affect birth date. The results suggest that severe inbreeding in moose has both indirect effects on fitness through delayed birth and lower juvenile body mass, as well as separate direct effects, as there still was a significant relationship between f and twinning rate after accounting for birth date and body mass as calf. Consequently, severe inbreeding as found in the study population may have consequences for population growth and extinction risk.     

A Systematic Review and Meta-Analysis of the Effect of Short Birth Interval on Infant Mortality in Ethiopia

IntroductionEven though Ethiopia has been celebrating the achievements of MDG 4, still one in every 17 Ethiopian children dies before their first birthday. This is the biggest of the African regional average. Short birth interval is inconsistently reported as a risk factor by limited and independent studies in Ethiopia. Therefore, the purpose of this meta-analysis was to determine the pooled effect size of the preceding birth interval length on infant mortality.MethodsStudies were accessed through the electronic web-based search mechanism from PUBMED, Advanced Google Scholar, WHO databases and journals: PLOS ONE, and BMC, using independent and combinations of key terms. Comprehensive meta-analysis version 2 was used to analyze the data. An I² test was used to assess heterogeneity. Funnel plot and statistical significance by Egger’s test of the intercept was used to check publication bias. The final estimate was determined in the form of odds ratio by applying Duval and Tweedie’s trim and fill analysis in the Random-effects model.Results872 studies were identified on the reviewed topic. During screening, forty-five studies were found to be relevant for data abstraction. However, only five studies fulfilled the inclusion criteria and were included in the analysis. In all of the studies included in the analysis, the preceding birth interval had a significant association with under-one mortality. The final pooled estimate in the form of the odds ratio for infant mortality with a preceding birth interval of less than 24 months was found to be 2.03 (95% CI: 1.52, 2.70, random effect (five studies, n=43,909), I²=70%, P<0.05).ConclusionIn Ethiopia, promoting the length of birth interval to at least two years lowered under-one mortality by 50% (95% CI: 35%, 63%).     

A ten-year summary of reproductive parameters for ring-tailed lemurs at berenty, madagascar

From 1989 to 1998, 204 live births were recorded for ring-tailed lemurs (Lemur catta) at Berenty, Madagascar. Excluding unknown birth dates, the peak month of birth was September, with 82.0% (146/178) occurring during this period. The offspring sex ratio (1∶1.19) was not significantly different from 1∶1, and there was no association with the mother's age. The first births occurred at the ages of 2 to 4 yr. The annual birth rate was very low at the age of 2 yr (11.1%), but increased thereafter: to 50.0% at the age of 3 yr, and to 75–85% at the age of 4 or more years. Multiple births were very rare, since only three sets of twins and one set of triplets were recorded. As for the interbirth interval, a one-year interval was the most common (92.2%). Infant mortality within the first year was 37.7% (77/204). Neonatal mortality within the first month accounted for 31.2% of all infant dealths.     

Productivity of Thai Brahman and Simmental-Brahman crossbred (Kabinburi) cattle in central Thailand

The productivity of the new crossbred cattle Kabinburi (K) was compared to that of Thai Brahman (TB) using 756 production records from K cattle and 1,316 production records from TB cattle kept at three locations in Thailand. The data were analyzed for the effect of breeds and locations. The ambient temperature, the humidity, the Temperature–Humidity Index (THI) and the rainfall of the three locations were different. Lamphayaklang Livestock Research and Breeding Center (LP) had the highest rainfall/year followed by Nongkwang Livestock Research and Breeding Center (NK), and Prachinburi Livestock Breeding Station (PC). Kabinburi cattle had a higher bodyweight at birth as well as at 200, 400 and 600 days of age than TB cattle. Furthermore, K heifers gave birth to their first calf at a younger age and had a shorter calving interval than TB cows. Thai Brahman cattle kept at LP had significantly higher bodyweight at 400 and 600 days than the animals kept at NK, but bodyweight at birth and 600 days of age were not significantly different. Thai Brahman cattle kept at LP were younger at first calving and had a shorter calving interval than the animals kept at NK. K cattle kept at NK were heavier at birth and at 200, 400 and 600 days of age than the animals kept at PC. Furthermore, Kabinburi cows kept at NK were younger at first calving (P < 0.01), but the calving interval was not different between the two groups kept at NK or PC.     

Rapid infant weight gain predicts childhood overweight

Objective : To determine among a contemporary cohort whether rapid weight gain between birth and 6 months is associated with risk of childhood overweight and if this risk differs by ethnicity and/or breast‐feeding history. Research Methods and Procedures : This was a cross‐sectional survey in 1999 to 2000 of parents/guardians of children participating in the Special Supplemental Nutrition Program for Women, Infants, and Children in New York State. Measurements were abstracted by chart review, including weight at birth and 6 months, and height and weight at time of survey and every 6 months subsequently. Overweight at 4 years of age was defined as a BMI ≥ 95th age‐ and sex‐specific percentiles. Results : The study sample was 32% Hispanic, 19% black, and 49% white; 17% of children were overweight. Rate of infant weight gain (expressed in terms of 100 g/mo) was significantly associated with being overweight at 4 years (odds ratio, 1.4; 95% confidence interval, 1.3 to 1.6 after adjusting for history of breast‐feeding, birth weight, and ethnicity). The odds of being overweight at 4 years of age for Hispanic children were twice those of non‐Hispanic children (odds ratio, 2.2; 95% confidence interval, 1.5 to 3.3). The population‐attributable risk of overweight at 4 years of age was 19% for children in the highest quintile of infant weight gain. Discussion : Among this contemporary, multi‐ethnic cohort, rapid infant weight gain was associated with increased risk of being overweight at 4 years of age, independently of potential confounders. Identification of the risk factors contributing to rapid weight gain during infancy might improve early recognition and guide strategies for optimal nutrition to prevent the development of childhood overweight.     

TAURINE IN THE BRAIN AND LIVER OF THE DEVELOPING HUMAN AND MONKEY

—The concentrations of taurine in brain and liver from human fetuses (2nd trimester) and adults and from Rhesus monkeys from mid-gestation, through birth and neonatal life to maturity have been measured. The concentration of taurine in human and monkey fetal brain was 4-5-fold higher than that in adult monkey brain. In human fetal brain the concentration of taurine decreased linearly with increasing crown-rump length (r=−0·75; P < 0·001). In fetal monkey brain, no correlation with gestational age was found. After birth, the concentration of taurine in monkey brain decreased linearly with increasing age (r=−0·96; P < 0·001) until values comparable to those found in the adult were reached 8-9 months after birth, approximately the end of weaning. The concentration of taurine in liver both from fetal humans and from fetal monkeys was approximately twice that in mature liver. Concentrations of taurine similar to those found in adult liver were reached within a few days of birth, compared to several months for brain. These results suggest that taurine may be associated with brain development in addition to any functional role it may play in the mature brain.     

Sexually dimorphic transitions revealed in the relationships of yearling rhesus monkeys following the birth of siblings

We report here that in a large captive group of monkeys, Macaca mulatta,sudden sex-related changes occur in social interactions in one short phase of an infant’s development. Social interactions of 1-year-old animals (males, N =12; females, N =8) 6 weeks before the birth of siblings were compared with interactions occurring 6 weeks after the birth. On the day of the siblings’ birth, depression-like postures were seen in two yearling males (YMs); 10 YMs showed hyperactivity. In the postbirth period, YMs refocused their attentions away from their mother and toward other, often unrelated members of the group. Although YMs initiated disengagement of interactions with their mothers, there was evidence that mothers attempted to lessen this disengagement. The YMs had close relationships with specific (“preferred”) male individuals. These relationships (particularly those with adult males) became more pronounced following the birth of the sibling. The adult-male group also took an active role in maintaining interactions with YMs. The preferred partners in the YM-other male relationship before the birth of the sibling were, however, not always the same as those in the period after the birth. Dominance relationships and probably genetic factors determined patterns of interaction between YMs and their preferred male partners. Among yearling females (YFs), no dramatic changes in interactions with their mothers or with other group members were detected after their mothers gave birth. Relationships in YF-mother and YF-other-individual pairs (especially when the other individual was kin) seemed to be consolidated during the postbirth interval. There was little evidence of jealousy between the YFs and their younger siblings. Thus, sibling birth acted as a stimulus for the occurrence of sexually dimorphic interactions in yearlings. We suggest that in natural environments, social interactions in YFs promote relationships that will serve to integrate them into the matrilineal social structure, whereas comparable behavior in YMs encourages relationships with males that they may emigrate with into, or meet again in, nonnatal troops.