Livestock production in central Mali: Reproductive aspects of sedentary cows

The results of a 6-year study of cow reproductive traits in an agro-pastoral system in semi-arid central Mali are reported. Age at first calving was 1505 days (49.5 months). Calving intervals averaged 665 days with a standard deviation of 202 days, but these showed a bimodal distribution centred on 13–16 and 23–26 months. Least squares analysis indicated that parturition number had a significant effect on the calving interval. Some 56% of calves were born in the period April to June, there being a very highly significant correlation between these births and rainfall 9 and 10 months previously. The average number of calves produced per cow in the herd was 2.9. Nutritional stress appears to be the main cause of low reproductive rates and of the seasonal pattern of births and mitigation of this stress would lead to higher calving percentages.     

On an extension of R.A. Fisher's result on the dynamics of the reproductive value

A classical result by Fisher concerning reproductive value dynamics is extended to the case of varying vital rates with a constant cohort Lotka's r. Based on the demographic potential approach, a generalization of the concept of reproductive value is introduced, which exhibits exponential dynamics both in the classical case of constant vital rates and in a wider class of populations. The generalized reproductive value introduced in this paper fits the classical interpretation by Fisher as a discounted sum of future births in the general class of models addressed here. Our results show when Fisher's classical results may be used as good approximations. They could also be of importance for estimating the fitness of biological populations, aggregate population modeling, and studying the long-term consequences of varying vital rates.     

Reproduction in the slender loris (Loris tardigradus malabaricus)

A breeding colony of slender lorises (Loris tardigradus malabaricus) was studied to obtain data for comparison with other prosimian species, to contribute reproductive information for improving management of captive lorises, and to resolve some uncertainties in the literature regarding reproduction in the slender loris. At the Duke University Primate Center, a female slender loris reached sexual maturity at approximately ten months of age and conceived at one year of age. The length of the estrous cycle was 29–40 days, with copulation occurring over two consecutive days during estrus. Gestation length was 166–169 days. Litter size for each six births was one. Conception did not occur during an immediate post-partum estrus, but four months after birth, resulting in a 9 1/2-month interbirth interval. There was no evidence of reproductive seasonality. Lactation lasted between five and seven months. Reproductive rates of slender lorises are among the lowest of primates less than 500 g. Differences in reproductive parameters may exist between different subspecies of slender lorises.     

Interannual variability in fruit abundance and the reproductive seasonality in Sumatran Long-tailed macaques (Macaca fascicularis)

In an environment with a seasonal food supply, most primate species show birth peaks which precede the peak food period by some two to five months. Sumatran Long-tailed macaques (Macaca fascicularis), however, showed birth peaks during or after the fruit peak. Years of high birth rates and early birth peaks alternated with years of low birth rates and late peaks. The timing of births was strongly influenced by a female's condition, which depends on food supply and her previous reproductive history. Pregnant females were more active than other females, whereas females with young infants were less active.
The unusual timing of births is ascribed to the unpredictability of the height of the annual fruit peak. This hypothesis is supported by the reproductive patterns of other South-east Asian primates and by a model comparing the two types of reproductive timing. Further differences between the two strategies of reproductive timing are predicted.     

On a Problem of Estimating the Female Foeticide and Infant Mortality Differential by Sex Based on Indirect Data

The paper develops a methodology to estimate the parameters concerning female foeticide and differential infant mortality rates by sex; for which direct data are difficult to be obtained. Therefore, appropriate modelling has been made enabling to estimate the above rates as well as other associated parameters (such as re‐conception rate in the early partities following a male or a female birth) from indirect data; such as data providing information on the interval between two male births or between a female and a male birth on the assumption there is a sex preference in favour of male children existing among the couples. The other type of data that may be used are on sex ratios at birth and at the first year of life. The working of the model has been illustrated by assuming certain conventional values for some of the parameters in the reproductive process as Post‐partum amenorrhoea (PPA), Gestation period and the sex ratios both natural as well as observed.     

Increment-decrement tables for human reproduction.

An increment-decrement life table method has been applied to family building patterns among women. Age at the occurrence of a specified birth is considered the principal duration variable. The data base used to illustrate the table method was a sample of currently married women from the 1965 U.S. National Fertility Survey. It is possible to calculate the average number of births occurring to a woman of given parity during any specific age interval. The average number of births occurring before age 25 for women who are childless at age 20 can be obtained by completing the reproductive history for 100,000 childless 20 year old women through age 25. In a sample of 86,242 first births, 51,425 second births, 17,485 third births, and 4755 fourth births for an average of 1.6 children before age 25. Summary measures such as average parity attained within a given age interval and the conditional probability of transition from one parity to the next in a given age interval can be calculated from a table providing the age intervals do not involve fractions of the age groups used in constructing the abridged table.     

On an extension of R.A. Fisher's result on the dynamics of the reproductive value

A classical result by Fisher concerning reproductive value dynamics is extended to the case of varying vital rates with a constant cohort Lotka's r. Based on the demographic potential approach, a generalization of the concept of reproductive value is introduced, which exhibits exponential dynamics both in the classical case of constant vital rates and in a wider class of populations. The generalized reproductive value introduced in this paper fits the classical interpretation by Fisher as a discounted sum of future births in the general class of models addressed here. Our results show when Fisher's classical results may be used as good approximations. They could also be of importance for estimating the fitness of biological populations, aggregate population modeling, and studying the long-term consequences of varying vital rates.     

Testing the weekend effect hypothesis: Time of day and lunar phase better predict the timing of births in laboratory‐housed primates than day of week

The weekend effect hypothesis proposes that captive primates are more likely to give birth during times of low disturbance and reduced staff activity. The hypothesis specifically predicts that laboratory‐housed primates will be more likely to give birth during the weekend than weekdays when staff activity is reduced. To date, support for the weekend effect hypothesis has been mixed and based on studies with relatively few subjects. To further examine the hypothesis, we analyzed the birthing patterns of three genera of laboratory‐housed primates: squirrel monkeys (Saimiri species, N = 2,090 births), owl monkeys (Aotus species, N = 479 births), and rhesus macaques (Macaca mulatta, N = 2,047 births). Contrary to predictions derived from the weekend effect hypothesis, the frequencies of births during weekends for all taxa were not significantly different from rates that would be expected by chance. However, while there was no variance across days of the week, all three taxa gave birth at nighttime, when staff was absent. This parallels reports of births in wild and captive monkeys, both diurnal and nocturnal, which are more likely to give birth during the night; plausibly a time when the environmental and social disturbance is lowest and the mother is safest to bond with her newborn infant. As all births occurred at night, we also explored the relationship between the lunar cycle and the timing of births timing. While the diurnal primates (i.e., Saimiri and Macaca) were no more likely to give birth on “bright” nights than “dark” nights, owl monkeys (Aotus) had a much higher frequency of births on bright nights than darker ones, and at rates that deviated from chance. Our data provide a more detailed understanding on how the environment may influence captive monkey births but do not support the oft‐cited weekend effect hypothesis.     

Reproduction of Angola free-tailed bats (Tadarida condylura) and little free-tailed bats (Tadarida pumila) in Malawi (Central Africa) and elsewhere in Africa

Angola free-tailed bats and little free-tailed bats occur in diverse habitats throughout most of Africa south of the Sahara. This study investigated the reproductive strategies and related biology of these species in Malawi where they were sympatric, and analysed data from elsewhere in Africa to show how the strategies varied along a gradient of habitats from approximately 12 degrees N to 25 degrees S. Both the Angola free-tailed bat and the little free-tailed bat were normally monotocous. Angola free-tailed bats invariably had 2 births/year, and the interval between consecutive births decreased with increasing latitude. When the interval was shortest (approximately 90 days) a post-partum oestrus occurred. Little free-tailed bats differed by having a shorter gestation (approximately 60 days), and the ability to have up to 5 births/year with a postpartum oestrus after each birth. The extent to which this potential is achieved varies with latitude and rainfall, mainly so that lactation can coincide with peaks in the abundance of food. The interaction between rainfall and reproductive characteristics results in the two species having patterns of reproduction which are sometimes similar, but more often different. Competition between the species is unlikely to be affected by differences in their reproduction.     

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.     

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.     

Reproduction of wild-caught marmosets (Saguinus labiatus labiatus) under laboratory conditions.

The reproductive performance of marmosets (Saguinus labiatus labiatus) was evaluated under laboratory conditions. Nineteen of 22 (86%) male-female pairs produced 32 live births during the first 18 months in the laboratory. The reproductive performance and survival rates were comparable to those of other Saguinus species maintained under similar conditions.     

Characteristic features of the reproduction of Koshima monkeys,Macaca fuscata fuscata: A summary of thirty-four years of observation

The reproductive data for Japanese monkeys,Macaca fuscata fuscata, which had been recorded for the 34 years from 1952 to 1986 on Koshima, were analyzed in terms of the influence of changes in artificial food supplies, the differences in reproductive success between females, the timing of births, and the secondary sex ratio. Koshima monkeys increased in number until 1971 when the population density was still small and artificial provisioning was copious. As described byMori (1979b), the severe reduction in artificial food supplies, which began in 1972, had an enormous deleterious effect on reproduction: the birth ratio of adult females of 5 years of age or more fell from 57% to 25%; the rate of infant mortality within 1 year of birth rose from 19% to 45%; primiparous age rose from 6 to 9 years old on average; and there was an increased death rate among adult and juvenile females. The prolonged influence of “starvation” may be seen in the significantly delayed first births of those females that were born just before the change in food supplies. When reproductive parameters are compared between the females who belonged to six lineages in the group during these periods, they were found to be rather consistent, although some individual differences can be recognized among females and subgroups. The apparent trend was that some of the most dominant females retained superior reproductive success while that of the second-ranked females has tended to diminish over the years since 1972. Such opposing trends were seen only in the most dominant lineage group and such a difference was not recognized among the females of other lineages. The difference in reproductive success is discussed in relation to both the different situations that arise because of the artificial food supplies and differences in feeding strategies. Multiparous females, after a sterile year, gave birth somewhat earlier than those who reared infants in the preceding year and, when artificial provisioning was intense, they tended to give birth a little earlier than during other periods. There is some evidence that the mortality of later-born infants was higher than that of earlier-born infants after 1972. However, this difference may not be responsible for the differential reproductive success of females since the timing of births did not differ among lineages. Furthermore, during the time when many females gave birth continuously, prior to 1972, the infant mortality did not differ with respect to the timing of births. The differences in infant mortality were not correlated with the reproductive history, parity or age of the mother, or with the sex of the infant. The secondary sex ratio varied by only a small amount, from slightly male-biased ratio (114: 100) when correlated with reproductive history, parity, age of mother, sex and survival ratio for preceding infants, timing of birth, and lineage of the female. Furthermore, the change in artificial food supplies did not cause any modifications of the secondary sex ratios, despite its enormous deleterious effect on reproduction. The secondary sex ratio of Japanese monkeys may not be influenced by the social factors mentioned.     

Timing and synchrony of birth in Eurasian lynx across Europe

The ecology and evolution of reproductive timing and synchrony have been a topic of great interest in evolutionary ecology for decades. Originally motivated by questions related to behavioral and reproductive adaptation to environmental conditions, the topic has acquired new relevance in the face of climate change. However, there has been relatively little research on reproductive phenology in mammalian carnivores. The Eurasian lynx (Lynx lynx) occurs across the Eurasian continent, covering three of the four main climate regions of the world. Thus, their distribution includes a large variation in climatic conditions, making it an ideal species to explore reproductive phenology. Here, we used data on multiple reproductive events from 169 lynx females across Europe. Mean birth date was May 28 (April 23 to July 1), but was ~10 days later in northern Europe than in central and southern Europe. Birth dates were relatively synchronized across Europe, but more so in the north than in the south. Timing of birth was delayed by colder May temperatures. Severe and cold weather may affect neonatal survival via hypothermia and avoiding inclement weather early in the season may select against early births, especially at northern latitudes. Overall, only about half of the kittens born survived until onset of winter but whether kittens were born relatively late or early did not affect kitten survival. Lynx are strict seasonal breeders but still show a degree of flexibility to adapt the timing of birth to surrounding environmental conditions. We argue that lynx give birth later when exposed to colder spring temperatures and have more synchronized births when the window of favorable conditions for raising kittens is shorter. This suggests that lynx are well adapted to different environmental conditions, from dry and warm climates to alpine, boreal, and arctic climates. This variation in reproductive timing will be favorable in times of climate change, as organisms with high plasticity are more likely to adjust to new environmental conditions.     

Month of birth predicted reproductive success and fitness in pre-modern Canadian women

Conditions experienced during early development affect human health and survival in adulthood, but whether such effects have consequences for fitness is not known. One surrogate for early conditions is month of birth, which is known to influence health and survival in many human populations. We show that in nineteenth century Canada, month of birth predicted a woman's fitness measured by the number of grandchildren produced, with the genetic contribution to the following generations by women born in different months differing by over seven grandchildren. This difference was mainly caused by differences in the reproductive rates of both mothers and their offspring, rather than differences in their survival. Women born in the best months of the year had longer reproductive lifespans, larger numbers of live births and raised more offspring to adulthood than those who were born in the worst months. Furthermore, the offspring of those women born in the best months also had greater reproductive rates, suggesting that month of birth also influenced a mother's ability to invest in her offspring. Our results suggest that early conditions may have important consequences for human lifetime reproductive performance within and between generations, and that timing of birth had large effects on fitness in this rural community.     

Reproductive patterns and birth seasonality in a South-American breeding colony of common marmosets,Callithrix jacchus

We analyzed data on captive-born and wild-caught females housed under natural conditions in a colony located in northeastern Brazil. No differences in reproductive performance were found between captive-born and wild-caught females. Twins were the most frequent litter size, followed by triplets and singletons. No parity effect was observed, with similar infant survival for nulliparous and multiparous females. No significant departures in sex ratio were detected for births and mortality of the male and female infants. The age of the females at the time of pairing showed a negative correlation with pairing-parturition length, but did not affect infant survival. The prolongation in pairing-parturition interval (PPI) and interbirth interval (IBI) was related to birth seasonality. The births were clustered in the second half of the dry season and the beginning of the wet season (November–March), and the time of pairing and the time of infant birth influenced the PPI and IBI, respectively. The use of outdoor cages, which allowed the animals to be aware of the seasonal variations in photo-period and rainfall seems to be sufficient to time the reproductive activity, even when the animals are maintained on a constant food supply.     

Cryopreservation of mammalian oocytes and embryos: current problems and future perspectives

Cryopreservation techniques for mammalian oocytes and embryos have rapidly progressed during the past two decades,emphasizing their importance in various assisted reproductive technologies.Pregnancies and live births resulting from cryopreserved oocytes and embryos of several species including humans have provided proof of principle and led to the adoption of cryopreservation as an integral part of clinical in vitro fertilization.Considerable progress has been achieved in the development and application of the cryopreservation of mammalian oocytes and embryos,including preservation of the reproductive potential of patients who may become infertile,establishment of cryopreserved oocyte banks,and transport of oocytes and embryos internationally.However,the success rates are still far lower than those obtained with fresh oocytes and embryos,and there are still obstacles that need to be overcome.In this review,we address the major obstacles in the development of effective cryopreservation techniques.Such knowledge may help to eliminate these hurdles by revealing which aspects need improvement.Furthermore,this information may encourage further research by cryobiologists and increase the practical use of cryopreservation as a major part of assisted reproductive technologies for both humans and animal species.     

Social organization, reproduction and rearing strategies of Callimico goeldii: new clues from the wild

The callitrichines are a specialized radiation of primates that are characterized in part by variable social systems and cooperative infant care. Callimico goeldii, unlike the other callitrichines, have single rather than twin offspring, reducing the need for allocare and permitting synchronous breeding within groups. Low mortality rates among offspring and unstable social groups are suggested to be possible factors that have led to single births among C. goeldii. Single offspring may benefit from greater maternal investment and more frequent food sharing than twin offspring, factors that may help to explain why C. goeldii reaches sexual maturity more rapidly than other callitrichines. In addition, increased breeding opportunities for young C. goeldii females may have selected for rapid maturation rates among this species. Postpartum ovulation and aseasonal resource availability appear to permit females to have biannual birth seasons, further increasing the potential reproductive output.     

Reproduction in high altitude Aymara: physiological stress and fertility planning?

Reproductive characteristics at high altitude are described based on the reproductive histories of 720 Aymara women, collected in 1998 and 1999 in a group of twelve peasant communities at a mean altitude of 4000 m in the Bolivian Altiplano. The reproductive pattern is shaped by a late onset of childbearing, associated with a rather short reproductive span and large birth intervals. Environmental conditions could explain the particularly late age at menarche of rural girls compared with their urban counterparts, whereas the age at first birth is likely to be under cultural control. The short reproductive span appears to result from a large mean interval between last birth and menopause, which is essentially determined by cultural decisions. The birth intervals, which are longer than in many traditional societies, could be the result of a slower restoration of postpartum fecundability induced by the hard way of life inherent in the Altiplano (including poor sanitary and nutritional conditions and high workload), perhaps aggravated by hypoxia. However, a secular trend in fertility is perceptible, towards earlier menarche, earlier age at first birth, increasing reproductive span and a slight increase in live births and surviving offspring, which is probably the result of a slow improvement in living conditions. The existence of birth control on the one hand, and a total fertility rate averaging six live births among the couples who do not practise contraception on the other, are other arguments against the hypothesis of a low natural fecundity in these Aymara groups.