Father Absence and Reproduction-Related Outcomes in Malaysia,a Transitional Fertility Population

Father absence is consistently associated with children’s reproductive outcomes in industrialized countries. It has been suggested that father absence acts as a cue to particular environmental conditions that influence life history strategies. Much less is known, however, about the effects of father absence on such outcomes in lower-income countries. Using data from the 1988 Malaysian Family Life Survey (n?=?567), we tested the effect of father absence on daughters’ age at menarche, first marriage, and first birth; parity progression rates; and desired completed family size in Malaysia, a country undergoing an economic and fertility transition. Father absence during later childhood (ages 8 to 15), although not during earlier childhood, was associated with earlier progressions to first marriage and first birth, after controlling for other confounders. Father absence does not affect age at menarche, desired family size, or progression from first to second birth. The patterns found in this transitional population partly mirror those in developed societies, where father absence accelerates reproductive events. There is, however, a notable contrast between the acceleration in menarche for father-absent girls consistently found in developed societies and the lack of any association in our findings. The mechanisms through which father absence affects reproduction may differ in different ecological contexts. In lower-income contexts, direct paternal investment or influence may be of more importance in determining reproductive behavior than whether fathers act as a cue to environmental conditions.     

Reproductive performance of Farafra ewes in the subtropics

The present study was carried out to assess the reproductive performance of Farafra ewes—a breed with potential economic importance in the subtropics. A total of 262 ewes were categorized according to age, parity, and postpartum interval. Ewes were introduced for breeding in fall, winter and late spring seasons. Fertility, prolificacy, lamb birth weight, and ultrasonic fetal parameters were recorded. Results obtained showed that litter size was increased with age and parity. Lamb birth weight was affected by season. None of the parameters studied had a clear-cut effect on fertility. However, an interaction between season and parity was detected. Measurement of fetal size in the first half of gestation did not predict birth weight. The obtained data represents the first record of the reproductive performance of Farafra ewes in the subtropics, which could be used to anticipate their performance in different seasons.     

Of chickens and eggs: diverging propagule size of iteroparous and semelparous organisms

Interactive effects of two or more life-history traits on fitness have the potential to create suites of coadapted traits. Propagule (egg or seed) size is one such trait that is believed to have undergone coadaptation with other traits. Phylogenetic analyses of salmonid fishes have revealed an association between large eggs and semelparity, leading to the question of which came first. It has been hypothesized that an increased egg size would have increased juvenile relative to adult survival, favoring a subsequent increase in reproductive effort and eventually semelparity. Others have suggested that this is insufficient to cause a shift in parity, implying to the contrary that semelparity gave rise to larger eggs. In a previous study we showed that environmental unpredictability might select for production of larger propagules. Here we use simulations to directly model how propagule size evolves in response to environmental unpredictability with varying degrees of iteroparity. Our results demonstrate that environmental unpredictability causes pronounced propagule size divergence between iteroparous and purely semelparous species in taxa with a fixed age at maturity (e.g., pure annual species). However, even rare incidents of repeat breeding are sufficient to reduce selection for larger propagules substantially and thus divergence. Furthermore, introducing variation in age at maturity within propagule size genotypes has evolutionary effects similar to that of repeat breeding. Environmental unpredictability is thus unlikely to provide a general alternative explanation for the observed egg size divergence between iteroparous and semelparous salmonids.     

Fathers, fat, and maternal energetics in a biparental hamster: paternal presence determines the outcome of a current reproductive effort and adipose tissue limits subsequent reproductive effort

Djungarian hamster females, Phodopus campbelli, are severely constrained in their ability to reproduce successfully and lose 20% of their body weight by the time pups are weaned. In the wild and in the laboratory, biparental care improves maternal reproductive success. Two experiments quantified the effects of paternal presence and partial lipectomy [surgical depletion of parametrial white adipose tissue (PWAT) on day 8 of the 18-day gestation] on maternal energy balance, reproductive success, and investment in a subsequent reproductive attempt. Paired females reproduced successfully, maintained body weight, and invested in a second litter. Removal of the male decreased pup survival, growth, and readiness for dispersal by 18 days of age. Solitary females lost 10% of their body weight by the birth and a further 10% by day 18 after the birth. Thus, paternal presence balanced maternal energy budgets during reproduction and prevented a 20% loss in body weight. Equivalent weight loss occurs in response to other maternal stressors, therefore 20% may be the maximum tolerable weight loss in this species. Fresh weight of interscapular brown adipose tissue was predicted by the extent of maternal hyperthermia but not by maternal energy balance or lipectomy. Partial lipectomy did not adversely affect the female or the first litter but decreased the probability of investment in a second reproductive attempt and halved the size of the second litter. This effect may have been due to the 0.1% of body weight amount of lipid removed or may reflect a specialized role for PWAT in adjusting maternal investment.     

The impact of reproduction on gambian women: Does controlling for phenotypic quality reveal costs of reproduction?

Life history theory predicts that where resources are limited, investment in reproduction will cause a decline in body condition and ultimately may lower survival rates. We investigate the relationship between reproduction and mortality in women in rural Gambia. We use a number of different measures of reproductive investment: the timing of reproduction, intensity of reproduction, and cumulative reproductive investment (parity). Though giving birth is clearly a risk factor for increased mortality, we find limited evidence that the timing, intensity, or cumulative effects of reproduction have a survival cost. Instead, there is some evidence that women who have invested heavily in reproduction have higher survival than women with lower reproductive investment: both high parity and late age at last reproduction are associated with high survival. The only evidence for any cost of reproduction is that women who have given birth to twins (considered a marker of heavy investment in reproduction) have higher mortality rates than other women, after the age of 50 years. A potential confounding factor may be differences in health between women: particularly healthy women may be able to invest substantially in both reproduction and their own survival, leading to the positive correlations between survival and both parity and age at last birth we observe. To control for differences in health between women, we reanalyze the relationship between reproduction and mortality but include variables correlating with health in our models (height, BMI, and hemoglobin). Even when controlling for health, the positive correlation between investment in reproduction and survival remains unchanged.     

The evolution of offspring size and number: a test of the Smith-Fretwell model in three species of crickets

Most models of parental investment in offspring assume a trade-off between propagule size and number, and an increasing concave down function relating offspring fitness to propagule size. In this study, we test these two fundamental assumptions, using three closely related species of crickets, Gryllus firmus, G. veletis, and G. pennsylvanicus. Egg weight, 35-day fecundity and 35-day egg biomass were estimated in a population of each species, and the relationships between these reproductive traits and date of egg laying and body size were estimated. The relationships between egg weight and offspring survival were also sought for eggs buried at different depths, soil moistures, and soil types (G. firmus and G. veletis), as well as in the field (G. pennsylvanicus). A trade-off between egg weight and 35-day fecundity was revealed in a multivariate analysis taking into account among-species variation in egg weight and body size. Independent of the environmental conditions affecting the eggs, a positive correlation existed between the number of larvae that emerged from the soil and propagule weight in each species. Therefore, these findings provide partial support for the assumptions considered in the models mentioned above. A single optimal egg size was favored in two out of the three sets of conditions in which the functions relating egg weight to larval survival could be derived. The conditions encountered by the eggs, however, influenced the average survival of the larvae, as well as the shape of the relationship between egg weight and offspring survival. This suggests that cricket eggs frequently face heterogeneous environments with respect to egg and hatchling survival; the implication of habitat heterogeneity on the evolution of an optimal egg size is considered. The relationships between the reproductive components and female age and size, as well as between egg size and variation in cricket life-history, are discussed in an ecological and evolutionary context.     

Size-dependent resource allocation among vegetative propagules and male and female functions in the forest herb Laportea bulbifera

Reproductive resource investment among vegetative propagules and male and female sexual function and their size-dependence were investigated in a perennial forest herb, Laportea bulbifera . A theoretical model based on fitness gain curves predicts that optimal investments in three reproductive modes will increase with plant size if fitness returns in all three modes increase but become saturated with investment. In a field population, large plants of L. bulbifera produced both male and female inflorescences with propagules, while small plants produced only vegetative propagules. Biomass of propagules, male inflorescences, and infructescences with achenes were all positively correlated with plant size. The increase in investment with plant size was larger for propagule production than for sexual reproduction. The relationship between propagule biomass and plant size was constant irrespective of year, while the relationship between the biomass of sexual reproductive organs and plant size differed between two successive years. Annual change of individual sex expression was investigated for 25 transplanted plants. Although each plant changed its sex expression variously among male, female and bisexual from year to year, 23 out of 25 plants produced both male and female inflorescences in at least one year. The number of viable (germinated and survived) offspring from seeds was not significantly different from the number from propagules. The production cost of a propagule was higher than that of a seed. Resource allocation theory does not seem to be applicable to size-dependent resource allocation, especially the allocation between seeds and propagules in this species.     

Effect of birth litter size, birth parity number, growth rate, backfat thickness and age at first mating of gilts on their reproductive performance as sows

The present study was performed to evaluate retrospectively the influence of birth litter size, birth parity number, performance test parameters (growth rate from birth to 100kg body weight and backfat thickness at 100kg body weight) and age at first mating (AFM) of gilts on their reproductive performance as sows. Traits analysed included remating rate in gilts (RRG), litter size, weaning-to-first-service interval (WSI), remating rate in sows and farrowing rate (FR). Data were collected from 11 Swedish Landrace (L) and 8 Swedish Yorkshire (Y) nucleus herds and included 20712 farrowing records from sow parities 1-5. Sows that farrowed for the first time during 1993-1997, having complete records of performance test and AFM, were followed up to investigate their subsequent reproductive performance until their last farrowing in 1999. Analysis of variance and multiple regression were applied to continuous data. Logistic regression was applied to categorical data. The analyses were based on the same animals and the records were split into six groups of females, i.e. gilts, primiparous sows, and sows in parities 2-5, respectively. Each additional piglet in the litter in which the gilt was born was associated with an increase of her own litter size of between 0.07 and 0.1 piglets per litter (P<0.001). Gilts born from sow parity 1 had a longer WSI as primiparous sows compared with gilts born from sow parity 4 (0.3 days; P<0.05) or parity 5 (0.4 days; P<0.01). Gilts with a higher growth rate of up to 100kg body weight had a larger litter size (all parities 1-5; P<0.05), shorter WSI (all parities 1-5; P<0.05) and higher FR (parities 2 and 5; P<0.05) than gilts with a lower growth rate. Gilts with a high backfat thickness at 100kg body weight had a shorter WSI as primiparous sows (P<0.001) compared with low backfat gilts, and 0.1 piglets per litter more as second parity sows (P<0.01). A 10 day increase in AFM resulted in an increase in litter size of about 0.1 piglet for primiparous sows (P<0.001) and a decrease (P<0.05) for sow parities 4 and 5.     

Optimal size and number of propagules: allowance for discrete stages and effects of maternal size on reproductive output and offspring fitness

Existing optimality models of propagule size and number are not appropriate for many organisms. First, existing models assume a monotonically increasing offspring fitness/propagule size relationship. However, offspring survival during certain stages may decrease with increasing propagule size, generating a peaked offspring fitness/propagule size function (e.g., egg size in oxygen-limited aquatic environments). Second, existing models typically do not consider maternal effects on total reproductive output and the expression of offspring survival/propagule size relationships. However, larger females often have greater total egg production and may provide better habitats for their offspring. We develop a specific optimality model that incorporates these effects and test its predictions using data from salmonid fishes. We then outline a general model without assuming specific functional forms and test its predictions using data from freshwater fishes. Our theoretical and empirical results illustrate that, when offspring survival is negatively correlated with propagule size, optimal propagule size is larger in better habitats. When larger females provide better habitats, their optimal propagule size is larger. Nevertheless, propagule number should increase more rapidly than propagule size for a given increase in maternal size. In the absence of density dependence, females with greater relative reproductive output (i.e., for a given body size) should produce more but not larger propagules.     

Maternal age, parity, and reproductive outcome in captive chimpanzees (Pan troglodytes)

As early as the 1970s, it was suggested that nonhuman primates may serve as models of human reproductive senescence. In the present study, the reproductive outcomes of 1,255 pregnancies in captive chimpanzees (Pan troglodytes) were examined in relation to parity and its covariate, maternal age. The results show that the percentage of positive pregnancy outcomes was negatively correlated with increasing parity. In addition, spontaneous abortions, stillbirths, and caesarian sections (C-sections) were positively correlated with increasing parity. Maternal age, rather than parity, was found to be the most important predictor of negative birth outcome. This study supports research demonstrating reproductive decline and termination in nonhuman primates, and is the first to quantitatively account for this phenomenon in captive female chimpanzees.     

Induced abortion ratio in modern Sweden falls with age,but rises again before menopause

A woman's reproductive value decreases over her reproductive life span and it is therefore predicted that the likelihood of termination of investment in a child decreases with increasing age. An eventual increase in termination ratio in the oldest age groups, as is often found in abortion statistics, could depend on older women on average having larger families rather than on age per se. We used data on abortions and births in Sweden during 1994 to investigate how abortion ratio is related to age and parity of women. We found that age-specific abortion ratio is U-shaped (i.e. that it is highest for the youngest and for the oldest age groups) in each parity class from zero to four children but that age-dependence breaks down in higher parity classes (5, ≥6). Thus, for each of the parity classes 0–4, the incidence of abortion decreases with age up to a point, but increases again as women approach menopause. This late increase in induced abortion ratio seems to depend on age per se. The data indicate that abortion ratio is an inverse function of fertility, and that investment in new reproduction gradually decreases as a woman approaches menopause. Assuming grandmothering as an important driving force in human life history evolution, such a pattern might indicate that the transition from behavioural investment in one's own children to one's grandchildren is a gradual process similar to the decline in ovarian function.     

Offspring size and timing of hatching determine survival and reproductive output in a lizard

Selection on offspring size and timing of birth or hatching could have important consequences for maternal investment strategies. Here we show consistent viability selection on hatchling body length across 2 consecutive years in a lizard that lays several clutches per season. There was no effect of hatching date on survival to maturity. However, both early hatching and large hatchling size increased adult size, which has a positive effect on total reproductive output. Earlier hatching also led to an earlier onset of reproduction. Overall, increased survival probability for large hatchlings and a positive effect of clutch size on recruitment suggest consistent directional selection on both egg size and clutch size within and across years. Because offspring size and timing of hatching are strongly affected by environmental and maternal effects, there should be potential for strong transgenerational effects on reproductive output in this species. We briefly discuss the implications of these results for the evolutionary ecology of maternal investment and population fluctuations in short-lived lizards.     

Congenital malformations and variations in reproductive performance in the ferret: effects of maternal age, color and parity

Demographic data of ferrets from a commercial breeding colony were analyzed for the effects of maternal age, parity and strain on reproductive performance and the frequency of gross congenital abnormalities observed at parturition. Litter size (mean +/- SEM) was found to be greatest for young, primiparous females (10.3 +/- 0.2) and decreased with advancing maternal age and parity to a cohort mean of 8.1 +/- 0.1 for third parity females 16 months of age. Age, parity or strain had no effect on 24-hour neonatal mortality (7%) or mortality from birth to weaning (20%) and an examination of the causes for death suggested that these rates can be reduced. The malformation rate from two cohorts of females whelping at different times of the year was low (less than 1.0%) and not significantly different. A higher frequency of malformed offspring was detected in females of low previous parity (0-2) than in those with three or more. Based on data obtained in this survey, the ferret would seem a valuable alternative, nonrodent species for teratologic investigations using currently recommended protocols.     

Age-related body weight constraints on prenatal and milk provisioning in Iberian red deer (Cervus elaphus hispanicus) affect allocation of maternal resources

Maternal phenotypic characteristics can influence key life history variables of their offspring through maternal effects. In this study, we examined how body size constraints on maternal weight in yearling and subadult compared to adult hinds (age class effects) affected prenatal (calf birth weight, calf to hind weight ratio) and postnatal (milk) provisioning of Iberian red deer calves. Age correlated with all prenatal and postnatal investment traits except calf gains, although correlations were weaker than those with maternal weight. Once the effect of linear increase in weight with age was removed from models, yearlings showed additional reductions in calf birth weight, calf gains, and milk provisioning. The low-calf birth weight might increase the risk of calf mortality during lactation, as this occurs primarily during the first day of life and is strongly related to birth weight. Yearlings showed a greater prenatal allocation of resources in terms of greater calf to hind weight ratio probably as an extra effort by yearling mothers to balance calf neonatal mortality. It might compensate young mothers to produce low-quality calves while still growing rather than waiting for the uncertain possibility of surviving to the next reproductive season.     

Maternal Investment of the Virunga Mountain Gorillas

The Trivers & Willard hypothesis (TWH) predicts that females with more resources should bias their maternal investment toward offspring of the sex that is most likely to benefit from those additional resources. This paper examines the sex allocation of 61 female mountain gorillas (Gorilla beringei beringei) of the Virunga volcanoes, Rwanda from 1967 to 2004. Like most highly dimorphic, polygynous mammals, mountain gorillas are expected to show greater variance in reproductive success among males than females, so mothers in good condition should bias their investment toward sons. Using dominance rank as the indicator of maternal condition, the TWH was tentatively supported by our results with interbirth intervals (IBI). Dominant mothers had longer IBI following the birth of sons, relative to the longer IBI that subordinate mothers had with daughters. In contrast, maternal condition did not have a significant effect on birth sex ratios. We also found no significant relationships with other variables that might influence birth sex ratios (e.g., maternal age, parity, or group size), and the overall birth sex ratio was not significantly different from a 50:50 split. Collectively, our results suggest that female mountain gorillas do not control the sex ratio of their offspring at birth, but they may adjust their subsequent maternal investment. This conclusion is consistent with recurring questions about whether any adjustments in birth sex ratios occur in primates.     

Age-specific changes in different components of reproductive output in female reindeer: terminal allocation or senescence?

Two different processes can lead to a change in individual reproductive output with age in long-lived iteroparous vertebrates. The senescence hypothesis predicts a decline of performance in old age, whereas the terminal allocation hypothesis predicts an increase. Using long-term (>30 years) individually based data of female reindeer, we first assessed age-specific variation in body mass and different components of reproductive output. Then we investigated the contribution of senescence and terminal allocation (the increase in components of reproductive output) processes for shaping observed patterns. We found that female reindeer body mass increased up to about 11.5 years of age, and decreased afterwards, supporting the senescence hypothesis. Calf birth mass, both in absolute terms or for a given female mass, first increased and then declined with female age, also supporting the senescence hypothesis. The female mass gain (June–September) decreased with increasing age, and female change in mass between 2 consecutive years decreased with female age, all patterns again supporting the senescence hypothesis. However, the autumn calf mass did not change with age. Calf body mass in autumn tended to be positively related to female mass gain, supporting a quality effect. Raising a calf had a marked negative effect on female mass gain, indicating energetic reproductive costs of raising a calf. Calf body mass in autumn did not influence yearly female mass change. Overall, our results provided consistent evidence for general effects of senescence on most components of reproductive output and highlighted that both individual heterogeneity and reproductive costs shape female reindeer reproductive tactics.     

The Particular Maternal Effect of Propagule Size, Especially Egg Size: Patterns, Models, Quality of Evidence and Interpretations

SYNOPSIS. Propagule size is perhaps the most widely recognizedand studied maternal effect in ecology, yet its evolution isnot well-understood. The large body of extant optimality theorytreats parental investment solely as an ecological problem,largely from the perspective of progeny. This approach has hadlimited success explaining the ubiquitous variation in propagulesize within and among natural populations at most temporal andspatial scales. This problem aside, an unassailable gap in propagulesize theory is that it pays little heed to the fact that offspringsize is a joint phenotype of two individuals- the offspringand its mother. Hence, the ecology of mothers is decidedly asimportant in shaping the evolution of propagule size phenotypes.There are two reasons to suspect that this gap may account forthe lack of success of optimality theory to explain variationin nature. The first is that optimality models of propagulesize make no allowance for, nor can they explain, widespread,multivariate correlations between maternal characters and clutchparameters, namely the positive phenotypic covariances of maternalage, size, fecundity, and per-propagule investment found inmany organisms. If per-propagule investment is optimized byselection based on the expectation of offspring fitness, thenwhy should that phenotype be a function of maternal age or sizewhen the ecological circumstances of progeny are not changingas a function of maternal age or size? The second gap in currenttheory is that, like all optimization theory, it is patentlynon-genetic in that it is assumed that the phenotypes optimizedare evolutionarily accessible. Recent maternal effects theoryindicates that traits subject to maternal influence behave inunanticipated ways. Specifically, there may be time lags inresponse to selection, and hence, selection away from the optimumphenotype. This paper explores a suite of issues pertainingto the evolution of propagule size from the broader perspectiveof propagule size as a maternal effect (PSME) with a goal ofwidening the lens through which propagule size is viewed byevolutionary ecologists. Two themes are developed. First, Isuggest that, to understand egg size variance and its implicationsfor both maternal and offspring fitness, it is necessary toconsider explicitly the ecological context in which a motheris producing eggs, not just that into which offspring will enter.I argue that some of the variables that have only been incorporatedin pairwise fashion (or not at all) into studies of propagulesize might account for the lack of agreement about how thisimportant life history feature evolves. Further, I suggest thatfailure to consider other sources of selection on maternal phenotypes,driven by a narrow adaptationist view that has historicallybeen taken of PSMEs, has obfuscated many interesting questionssurrounding their coevolution with maternal characters. Thus,the second theme is that it is necessary to consider other explanationsfor why prop-agule size varies apart from those pertaining tooffspring fitness per si. Based on a detailed review of theempirical literature, I conclude that the concept of an optimalpropagule size is not only an insufficient construct to explainthe evolution of propagule size, but that continued relianceon an optimization approach is likely to stifle developmentof more realistic and predictive theory for the evolution ofthis key life history trait. Novel theory should incorporaterealities from physiology, development and genetics and shouldaccommodate the dynamic nature of the selective environmentsin which propagule size evolves, all of which have been shownby empiricists to play a role in determining propagule sizephenotypes. A key feature of this theory should be the explicittreatment of propagule size as a maternal effect.     

Age‐Related Male Reproductive Investment in Courtship Display and Nuptial Gifts in a Moth,Ostrinia scapulalis

Due to a trade‐off between current and future reproduction, costly reproductive investments should be increased towards the end of a lifespan when the probability of reproduction becomes low (terminal investment hypothesis). We investigated age‐related changes in male reproductive investment towards courtship display and the spermatophore in three age classes (young, middle‐aged and old) of a monandrous moth, Ostrinia scapulalis. As predicted, old males had higher mating success than young and middle‐aged males in no‐choice tests. Moreover, two‐choice tests revealed that middle‐aged males had a higher success rate than young males because of their higher courtship frequency rather than any female preference for them. It was found that old males produced a larger spermatophore than young and middle‐aged males, suggesting greater reproductive effort. The protein content of spermatophores also tended to increase with male age. Despite the age‐related variation in spermatophore size and protein content, age did not affect female fecundity or longevity. A decrease in the number of sperm in the older males might counteract the nutritional benefit of larger spermatophores. Alternatively, fitness components other than longevity and fecundity may be influenced by male age.     

Calling,Courtship, and Condition in the Fall Field Cricket,Gryllus pennsylvanicus

Theoretically, sexual signals should provide honest information about mating benefits and many sexually reproducing species use honest signals when signalling to potential mates. Male crickets produce two types of acoustic mating signals: a long-distance mate attraction call and a short-range courtship call. We tested whether wild-caught fall field cricket (Gryllus pennsylvanicus) males in high condition (high residual mass or large body size) produce higher effort calls (in support of the honest signalling hypothesis). We also tested an alternative hypothesis, whether low condition males produce higher effort calls (in support of the terminal investment hypothesis). Several components of long-distance mate attraction calls honestly reflected male body size, with larger males producing louder mate attraction calls at lower carrier frequencies. Long-distance mate attraction chirp rate dishonestly signalled body size, with small males producing faster chirp rates. Short-range courtship calls dishonestly reflected male residual mass, as chirp rate and pulse rate were best explained by a curvilinear function of residual mass. By producing long-distance mate attraction calls and courtship calls with similar or higher effort compared to high condition males, low condition males (low residual mass or small body size) may increase their effort in current reproductive success at the expense of their future reproductive success, suggesting that not all sexual signals are honest.     

Dominance Rank and Parental Investment in Swine (Sus scrofa domesticus)

Using domestic swine, we tested the general prediction from life history theory that females increase their investment in offspring with increasing age and parity. Because increased investment may have a greater beneficial impact on the lifetime reproduction of sons than daughters, we also tested the prediction that older females would invest more in sons than in daughters compared to younger females. Finally, we examined whether age- or parity-related patterns of change in reproductive effort were associated with differences in the social dominance ranks of females. Female swine from a large number of domestic breeds were assigned to social groups, and their dominance ranks were determined based on the outcome of agonistic encounters. The prediction that older females produce larger litters was supported, but the increase was related only to age, not to parity. Across all ages, high-ranking females produced a greater proportion of sons than low-ranking females. Contrary to our prediction, there was no rank-related change in the proportion of sons born with increasing age or parity. However, the mean body masses offspring born to high-ranking females increased with increasing maternal age and parity, but this was not the case for offspring of low-ranking females. Studies of free-ranging groups of swine are needed to determine whether an increase in body mass at birth would have different effects on the reproduction of sons or daughters.