Reproductive Parameters and Maternal Investment in Mandrills (Mandrillus sphinx)

We report on 14 years of reproductive data for semifree-ranging mandrills (Mandrillus sphinx) in Gabon, and we explore relationships between female rank, age and parity, and reproductive strategies. Most births (61% of 132) occurred during the wet season in Gabon, between January and March. Female rank and parity were unrelated to the timing of parturition. Gestation lengths average 175 days (SE = ±1 day; N = 61) and were similar irrespective of female rank, parity, or sex of offspring. Birth sex ratio did not differ significantly from unity (52% male), and was unrelated to maternal rank or parity. Stillbirths and neonatal mortality tended to be more common among lower-ranking females than among either mid-ranking or dominant females. Median age at first birth is 4.71 years, at a median body mass of 7.6 kg, ca 5 years before females attain their adult body mass (median 12 kg). Age at first reproduction is significantly correlated with dominance rank, with dominant females giving birth on average 1.3 years earlier than lower-ranking females do. Interbirth intervals (IBI) average 405 days (range 184–1159 days, N = 103), and are independent of the sex of the offspring. Infant death within 6 months shortened IBI to 305 days. Increasing age and parity are also associated with short IBI, as is higher rank. Maternal rank and parity appear to influence reproductive success in female mandrills, but there is no apparent differential maternal investment by sex.     

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.     

Reproductive seasonality in a free-ranging troop of stumptail macaques (Macaca arctoides): A five-year report

Seasonality in births and fertile matings are reported for a stumptail macaque group living on an island for a period of five years: 1975–1979. During this period 26 births occurred of which 24 represent infants conceived on the island. While births and fertile matings occurred throughout the year 21% of the births were concentrated in March, 34% in June and July and 17% in November. Additionally 63% of the births occurred during the rainy season. Of the 24 infants, 4 died during the first year of life thus yielding a reproductive success of 83%. The sex ratio at birth for the five years was 1:1 corrected to 1:1.2 with the four deaths. The mean interval between fertile matings for females was 19 months and 2 days and the mean age for first conception was 4 years and 5 months. The pattern of birth and breeding seasonality was markedly similar to that of the parent troop while in Puerto Rico.     

Reproductive parameters of wild female Rhinopithecus roxellana

On the basis on 6 years of observation, we estimated the reproductive parameters of a Golden snub-nosed monkey (Rhinopithecus roxellana) group in the Qinling Mountains, China. We observed 88 births in 47 females from 2001 to 2006. Two methods were used to calculate the birthrate. The first method is based on the number of births observed in a year, giving 0.49+/-0.07 (mean+/-SD), and the second method is based on the female-years of observation, giving 0.49+/-0.17 births per female per year in this troop. The mean interbirth interval is 21.88+/-6.01 months (mean+/-SD). The mortality of infant born between 2002 and 2005 was 22.4%. The interbirth intervals of females that had lost an infant before the age of 6 months were significantly shorter than that of females whose infants survived for more than 6 months. A female usually gives birth once every 2 years if the previous offspring survives to a weaning age of 5-6 months, or will give birth in the next year if the previous young dies before reaching an age of 6 months. Births were significantly concentrated during March to May of each year. The mean birth date was on April 14, median was April 12; and the standard deviation was 13.98 days. Birth peak occurs 6-7 months after mating peak. From observations on 15 individuals that gave birth for the first time, we concluded that the wild female Golden snub-nosed monkeys in Qinling Mountains start giving birth at an age of 5 or 6 years. We suggest that the seasonal reproductive pattern is an adaptive response to the availability of seasonal food. Our results are consistent with the hypothesis that these reproductive characteristics are a result of adaptation to the seasonality of mountain climate and food resources.     

Reproduction in captive lion tamarins (Leontopithecus): Seasonality,infant survival,and sex ratios

Diversity in reproductive and social systems characterizes the primate family Callitrichidae. This paper contributes to our appreciation of this diversity by presenting the first detailed comparative analysis of captive breeding in three species of lion tamarins (Leontopithecus chrysomelas, L. chrysopygus, and L. rosalia) housed at the Centro de Primatologia do Rio de Janeiro. The annual pattern of reproduction in all three species of Leontopithecus was markedly seasonal, with births occurring during the spring, summer, and fall months from August through March. While modal number of litters produced per female per year was 1, approximately 20% of breeding females produced two litters per year. The onset of breeding activity in years when two litters are produced was significantly earlier than in years when only one litter was produced. The cumulative number of offspring surviving to 3 months of age did not differ between years with one vs. two breeding attempts. Like other callitrichids, postnatal mortality was highest during the first week of life, and there were pronounced species differences in offspring survival through 1 year, with significantly lower survivorship in L. chrysomelas. Infant survivorship was affected by a number of experiential factors. Survivorship up to 30 days of life was higher in groups in which the breeding female had previous experience with infants as a nonbreeding helper than in groups in which the female lacked previous helping experience. Likewise, survivorship to 30 days of life was higher for infants born to multiparous females than for infants born to primiparous females. When parity and previous helping experience were analyzed concurrently, the lowest survivorship was associated with offspring produced by inexperienced primiparous females. Genus-wide, there was no significant departure from a 50:50 sex ratio at any point during the first year of life, nor was there evidence for differential mortality for male and female infants. However, L. chrysopygus produced significantly more male infants at birth (65:44) and had male-biased litters (approximately 60% males) throughout the first year of life, while L. chrysomelas showed a nonsignificant tendency toward female-biased litters. © 1996 Wiley-Liss, Inc.     

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.     

Reproductive performance of a laboratory breeding colony of patas monkeys (Erythrocebus patas)

Reproductive statistics were gathered over a 5½-year period on a colony of Erythrocebus patas. Pregnancies occurred throughout the year under laboratory conditions with a suggestion of a mating peak in the late fall and early winter. Menstrual cycles were monitored and found to average 30.6 days in length. Maximal vaginal cornification occured on day 15 of the cycle suggesting a midcycle ovulation. However, production of timed-mated pregnancies indicated ovulation occurred earlier and that breeding on days 10, 11, and 12 after menstruation was more likely to result in pregnancy. The gestation length was found to average 167.2 days in 142 harem-bred females and 167.5 days in 11 timed-mated pregnancies. Sixty-two percent of all pregnancies resulted in live births; 28% of the conceptions terminated with in-utero death of the fetus. Stillborn infants were delivered in 9% of the pregnancies. Infant mortality during the first 6 months of life was 10.2%. Females raised in the colony conceived their first offspring at approximately 3 years of age and males were able to sire infants at 3 years and 8 months.     

Determinants of fecundity and reproductive success in captive vervet monkeys

Between 1975 and 1983, adult female vervet monkeys (Cercopithecus aethiops sabaeus) over 3.5 years of age, living in two undisturbed social groups in a captive colony in Sepulveda, California, have averaged 1.0 births per female year with a mean interbirth interval of 10.7 months. Increased fecundity did not result in decreased survival rates of offspring in this population. Fecundity was influenced by the mother's age and dominance rank. The primary factor in the age-fecundity relationship was the age at first birth, which varied from three to five years. High-ranking females contributed the most to the high rate of fecundity, with significantly shorter interbirth intervals, more births per female year, and more surviving infants compared to low-ranking females.     

Reproductive biology of captive Arabian oryx (Oryx leucoryx) in Saudi Arabia

Reproductive data on captive Arabian oryx (Oryx leucoryx) were collected from June 1986 through April 1992 at the National Wildlife Research Center (Taif, Saudi Arabia). Oryx females are polyestrous. The estrous cycle averaged 22 days and mean gestation length was 260 ± 5.5 days (S.D). Sex ratio at birth was unbiased and mean weight was 6.5 ± 0.7 kg (S.D.), with no difference between sexes. Under captive breeding conditions, births occurred throughout the year. Females gave birth to a single calf at any time during the day and produced 1.03 young per year. Abortion rate was 3.6%. Mortality rate of young was 6.1% before weaning at 3 months of age. The interbirth interval averaged 295 ± 42 days (S.D.), with 53% lasting between 270 and 279 days. Females reached sexual maturity at the age of 13 months. © 1996 Wiley-Liss, Inc.     

Reproduction of the lesser kudu (Tragelaphus imberbis) at Dvůr Králové Zoo

Reproductive data on captive lesser kudus (Tragelaphus imberis) were collected from 1972 to 1990. The estrous cycles of two females were 21 and 22 days. Mean gestation length of 18 pregnancies was 244 ± 5.5 days (range = 235–256 days), and 71.2% of interbirth intervals (n = 146) were from 248 to 365 days. Births occurred throughout the year, but 55% were from September to December. Females always gave birth to a single calf (n = 215), and the sex ratio did not differ from unity. Neonatal weights (1–3 days postpartum) of 32 males and 28 females surviving at least 30 days were 6.4 ± 0.8 kg and 5.8 ± 0.7 kg, respectively. Males and females reached sexual maturity at the ages of 16 and 19 months, respectively. The oldest male lived to slightly more than 14 years, 5 months, and the oldest female to more than 18 years, 11 months. Males were fertile until at least 14 years and females minimally to 14–18 years of age; however, the maximum age of successful lactation was 13–14 years. © 1992 Wiley-Liss, Inc.     

藏酋猴社群雌体的性行为模式

猕猴属中大部分种类的繁殖类型可划分为季节性繁殖和非季节性繁殖两大类型。但是藏酋猴全年均有交配行为发生, 而产仔仅在1～8月间, 其类型属特殊的非季节性交配-季节性产仔繁殖类型。藏酋猴雌性在妊娠后选择的交配对象主要是高序位的雄性, 但非妊娠雌性则主要选择低序位雄性。妊娠后的雌性交配频率低于非妊娠雌性, 同时它们与成年雄性间理毛行为的发生频率亦低, 反之受到成年雄性攻击的频率却高。     

Reproductive parameters of a captive colony of capuchin monkeys (<Emphasis Type="Italic">Cebus apella</Emphasis>) from 1984 to 2006

This paper presents the results of a demographic analysis of 22 years of data recorded on a colony of tufted capuchin monkeys (Cebus apella) in captivity at the CNR Primate Centre (Rome, Italy). Information is provided on reproduction, sex ratio, inter-birth interval (IBI), seasonality, and body weight. From 1984 to 2006, 46 live births were recorded. There were births in almost all months of the year, but a higher frequency was observed during spring and summer (71.1%). The sex ratio was 1:1 M:F for newborns and 1:1.06 M:F for surviving offspring. At birth, infants’ average weight was 238.13 ± 37.51 g, i.e. 250 ± 56.79 g for males and 231 ± 26.08 g for females. Age at first birth for females ranged from 4.9 to 7 years (n = 9), while males achieved first paternity between the ages of 5 and 9.2 years (n = 6). Only one pair of twins was recorded during this period. For females, the mean IBI was 17.88 ± 1.84 months, when they reared infants, and 12.70 ± 1.73 months, when they did not rear offspring. Infant mortality within the first 2 months was 28.3%.     

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.     

Reproductive parameters of clouded leopards (Neofelis nebulosa)

Reproductive data compiled from the International Clouded Leopard Studbook revealed that 75% of all litters were born to females between one and five years of age. Sixty-three percent of the males had sired litters by four years of age with reproduction declining after six years of age. Sixteen zoological institutions surveyed worldwide contributed estrous cycle data from 28 clouded leopards. Sexual maturity (age at first estrus) for these females ranged from 17 to 28 months of age with a mean estrous cycle length of 29.9 ± 13.8 days. The mean length of estrus was six days. Gestation length ranged from 85 to 121 days (X? = 93.4 ± 6.3). There was a significantly higher incidence of estrus in fall and winter compared with spring and summer over latitudes ranging from 36°–45° and 51°–55° (P < .005). Mating occurred in all months except June and October, and cubs were produced in all months except December. The highest frequency of mating occurred during the month of December corresponding with a birth peak in March.     

海南岛南湾半岛野生猕猴的繁殖研究

1981-1985年,在海南岛南湾半岛开展了对野生猕猴种群繁殖的研究。猕猴的发情交配期为11月至次年3月,产仔期为4-8月,怀孕期约177天。3年中,有70%的性成熟母猴每年产1胎,其它的产2胎或1胎。在连续两年中产仔间隔294-441天,平均362±16天,自1978年以来,年均繁殖率为53.8-100%,平均77.8±13.85%。雄性成熟年龄为3-4岁;约38%的雌性在3.5岁时开始怀孕,4岁产仔。低等级的雌性生育较少,雄性猴离群,无任何雄性终身在群内称王,这些都可避免种群衰退,利于种群生长和发展的极好生物学对策。     

Birth seasonality and interbirth intervals in free-ranging formosan macaques,Macaca cyclopis, at Mt. Longevity, Taiwan

Thebirth season of Formosan macaqueM. cyclopis during our study started in February and ended in August with a peak in the second half of April and the first half of May. The average birth rate was 82%±21 for 114 females with four years of breeding records. Our study reports that a time span of one year between births can be considered as the norm for the wildM. cyclopis. Of the 288 inter-birth intervals (IBI), 88.5% showed a 1-year interval (mean 364±SD 29 days); 11% showed 2-year interval (727±36 days); and 1% (2 females) had 3-year interval (range 1030–1040 days). The IBI for females that had infant loss within six months of life were the shortest. But there was no significant difference from that of females that had stillbirth (p>0.9) and infant that survived for first six months of life (p>0.06). However, among 255 cases of 1-year IBI, stillbirth or following infant loss within six months of life did significantly shorten IBI for ten days (F _1,253=5.74,p<0.05).     

Age specific fecundity,litter size,and sex ratio in the chacoan peccary (Catagonus wagneri)

Ten years of data on the reproductive biology of the Chacoan peccary (Catagonus wagneri) were analyzed to determine average litter size, sex ratio, timing of births, and individual and age-specific fecundity. Data were obtained from a captive herd of chacoan peccaries located in the western Paraguayan Chaco. Births peak in the austral spring months of September, October, and November, with fewer litters born during the dry season months of June, July, and August. The average litter size was 2.4 with a sex ratio of 56:44 (M:F). There was no significant difference in litter size among individual females or among females of different ages. Finally, there was some individual variation in the age at which sows produced their first litter, but no discernible variation among sows in the average time between litters. Zoo Biol 16:301–307, 1997. © 1997 Wiley-Liss, Inc.     

Estimates of reproductive parameters for free-rangingAteles geoffroyi

Six and a half years of data collected on the reproductive parameters of a population of free-rangingAteles geoffroyi show the following characteristics: seasonality of births; interbirth interval of ca. 32 months; nursing by infants for more than 2 years; and reproductive life span of females continuing beyond 20 years of age. These characteristics appear to reflect adaptations to a primary resource base, ripe fruit, that is very low in protein and patchily distributed in space and time in tropical forests.     

Environmentally cued parturition in a desert rattlesnake,Crotalus atrox

Embryonic development in animals is dynamically regulated by physiological, behavioural, and environmental factors (temperature, precipitation, humidity), which in turn influence the timing of birth or hatching. In the present study, we provide evidence that parturition in a large‐bodied North American pitviper, the western diamond‐backed rattlesnake (Crotalus atrox), is environmentally cued. Specifically, we tested the hypothesis of births coinciding with rainfall events during the second‐half of the monsoon season (late July to mid September) using randomization modelling. Twenty‐one adult females surgically implanted with radio‐transmitters were tracked for extended periods from 2001–2010. From 2003 to 2007, the 21 females gave birth to 38 litters, generating sufficient data to test our hypothesis. In all years, births were restricted to a 4‐week period from 5 August to 7 September, which spanned between 6 and 19 days (mean ± SD, 15 ± 5.2 days). Most births (92.1%) occurred in August. Births were significantly associated with rainfall events in 2007, although births in 2003 and 2005 occurred closer to rain events than randomly generated births for respective years. However, when birth events across all 5 years were pooled, the model indicated a significance difference in mean rain‐days versus random rain‐days. Hence, births occurred more closely to rain events than random days. Other variables associated with monsoon events (increases in cloud cover and humidity; changes in barometric pressure) were not measured but constitute potential cues. The present research is the first long‐term, individual‐based radio‐telemetric study of a snake species to investigate environmental cues related to parturition using procedures of randomization modelling. © 2013 The Linnean Society of London, Biological Journal of the Linnean Society, 2013, 110 , 866–877.     

Life history of yellow baboons: Physical development,reproductive parameters,and infant mortality

Longitudinal data from a population of yellow baboons,Papio cynocephalus, in the Amboseli National Park, Kenya, provide life history parameter estimates. Females reached menarche at approximately four-and-a-half years of age and then cycled for approximately a year before first conception. Postpartum anestrum averaged 12 months but ranged from six to 16 months. In cases of still births or infant death during postpartum amenorrhea, females commenced cycling after approximately one month. In mature females the time spent cycling before conception was five months on the average with a range from one to over 18 months. Only half of all full-term pregnancies resulted in infants who survived the first year of life; only a third, in infants who survived until the birth of their mother’s next infant. In comparison with data from laboratory colonies, our data indicate that female baboons in Amboseli are older at birth of first infant. They have, on the average, a somewhat shorter interbirth interval than was estimated from earlier crossectional field data, and therefore spend a larger portion of their adult life pregnant, but have a much longer interval—at least three years on the average—between the birth of an infant and the birth of that infant’s next older surviving sibling. A number of morphological changes in immature baboons are described.