Social rank, fecundity and lifetime reproductive success in wild European rabbits (Oryctolagus cuniculus)

Wild European rabbits of both sexes have separate linear rank orders, which are established and maintained by intensive fights. This paper presents data from a 14-year study (1987-2000) on the population physiology and behavioural ecology of wild rabbits living in a 22,000 m² enclosure and focuses on the relationship between social rank and reproduction in females. Group composition, social ranks, fecundity and reproductive success were known for all females (n=197) from the outset of their first reproductive season at an age of about 300 days until their death. The annual reproductive success of females was influenced to a large extent by their social rank. This depended on two effects of about equal strength: a higher fecundity of high-ranking females and a lower mortality of their offspring between birth and adulthood. The lifetime reproductive success of the females varied greatly. Only about 50% of all females had any reproductive success (range: on to nine adult offspring). The social rank achieved by the females during their first reproductive season substantially influenced their lifetime reproductive success: The mean reproductive lifespan and lifetime fitness of high-ranking females (ranks 1 and 2) was about 60% greater than that of lower-ranking females, although many of the latter also gained dominant positions in subsequent years.     

The demographic consequences of the cost of reproduction in ungulates

The cost of reproduction can generate covariation between demographic rates that can potentially influence demography and population dynamics in long-lived iteroparous species. However, there has been relatively little work linking the survival cost of reproduction and population dynamics. The apparent scarcity of information on this important link is potentially due to covariation between vital rates, which can substantially influence fluctuations in population size. In this paper we examine the opportunity for survival costs of reproduction to leave a dynamic signature using a simulation model based broadly on an ungulate life history. We find that an increase in the cost delays the onset of reproduction and reduces reproductive rates of young, but not of prime-age, females. Accordingly, the number of offspring produced declines and the interval between reproductive events increases among young females experiencing high cost. These effects are translated to an age structure skewed toward young ages and reduced population density. These results suggest that, by delaying reproduction when conditions deteriorate, females protect their survival during the critical first three years of life, after which the negative effect of reproduction on survival declines. Unless conditions for reproduction are severe, it is not profitable to delay reproduction beyond age 3 years due to the high risk of death before having a chance to reproduce. We also demonstrate that lack of adjustment of reproductive strategies to elevated levels of the cost of reproduction, for example due to rapid changes in environmental conditions, results in lower average density and longevity compared to females that have sufficient time to adjust to changes in the cost. This suggests that even moderate costs of reproduction may have a major negative effect on population dynamics of ungulates.     

Dominance rank,resource availability,and reproductive maturation in female savanna baboons

Summary Ten years of data collected from a population of savanna baboons, Papio cynocephalus anubis, residing near Gilgil, Kenya were analyzed to ascertain the extent to which social and ecological factors influence reproductive maturation in females. First sexual swelling occurred at an average age of 4.79 years and first birth occurred at an average age of 6.92 years. Age at first menses was significantly correlated with age at first sexual swelling, but age at first sexual swelling was not a good predictor of age at first birth. The amount of rainfall in the 6 months preceding first sexual swelling and resource availability were significantly correlated with age at first sexual swelling. When ecological factors were taken into account, dominant females had an earlier age at onset of puberty, but not an earlier age at first birth, than did subordinate females. We suggest that nutritional and social stress operate at the same physiological level to disrupt GnRH pulsatility and retard reproductive maturation in some females. Given that socioecological variables modify the timing of life history events related to fitness in female baboons, the task for the future is to unravel how socioecological factors influence different life history components and generate variation in lifetime reproductive success. Correspondence to: F.B. Bercovitch     

Age-specific survivorship in relation to clutch size and fledging success in California gulls

Summary Data from a natural population of California gulls (Larus californicus) demonstrated that increasing reproductive effort with age was associated with reduced survivorship. Number of offspring fledged but not clutch size was inversely related to adult survivorhip indicating that reproductively induced mortality resulted from the cumulative effects of the entire breeding season. Agerelated increases in fledging success were correlated with increased adult mortality. Young gulls fledged few offspring and had high survival rates. Old gulls tended to fledge more offspring and had low survival rates. However, those old gulls fledging few offspring survived as well as young gulls. Data also invalidate the assumption that survivorship is age-constant in this species.     

Lifetime mating success, sexual selection and life history of fallow bucks (Dama dama)

We used data from a long-term study (15 years) of fallow deer to report for the first time the lifetime mating success, overall variance in lifetime mating success, and age-specific mortality levels of males. Fallow bucks that gain matings have higher social dominance rank, higher rates of fighting, and invest more in vocal display during the breeding season than unsuccessful males. Therefore, we examined if mating was associated with trade-offs in terms of survival, lifespan, and mating potential. We found that the variance in lifetime mating success was very high: 34 (10.7%) males mated, and of those, the 10 most successful males gained 73% of all matings (n=934). Mortality rates were generally high and only 22.3% (71/318) of males reached social maturity, i.e., 4 years. The oldest male was 13 years old. We found that fallow bucks that mated were not more likely to die during the following year, did not suffer from a reduction in lifespan, and did not incur lower mating success later in life as a result of mating during the early years of social maturity. Our results show that mating males at age 5 years (and possibly 9 years) may be more likely to survive than non-mating males. Additionally, the number of matings gained by males during the first years of social maturity was positively correlated with lifespan. We suggest that mating males are of higher quality than non-mating males because they are not more likely to incur trade-offs as a result of their increased reproductive efforts. Received: 9 November 1999 / Revised: 30 April 2000 / Accepted: 27 May 2000     

Life history consequences of variation in age at primiparity in northern elephant seals

Summary The age when female northern elephant seals, Mirounga angustirostris, bear their first young varies from 2 to 6 years. At Año Nuevo, California, a group of 77 females, primiparous at age 3, had a lower survivorship rate to each successive year up to age 8 than a group of 98 females that deferred initial pupping until age 4. The difference in survivorship appears to be due to the greater relative energetic costs of gestation and lactation incurred by the earlier breeding females during a period in their development when growth is rapid. An alternate hypothesis for the difference in survivorship — that young primiparous females are in poor condition from birth-is untenable; females that pupped early in life were larger at weaning age (a correlate of condition) than females that were primiparous 1 year later.Models based on the data show that differential survival of seals that vary in age at primiparity has important consequences for population growth and life history strategies. The effect of age at primiparity on the rate of increase of populations varies with colony density and juvenile survivorship. The optimal life history strategy for female elephant seals under most conditions existing today, including those at Ano Nuevo during the study period, is to bear the first offspring at age 4. Primiparity at age 3 is projected to be favored when harem density is very low and weaning success and juvenile survivorship are high; postponement of first breeding to age 5 is expected at high harem densities with intense competition for breeding space. Offprint requests to: B.J. Le Boeuf     

Multiple socioecological factors influence timing of natal dispersal in kangaroo rats

Natal dispersal is an important event in the life history of many species. Timing of natal dispersal can influence survivorship and subsequent reproductive success. A variety of individual proximal factors determine if and when offspring disperse from the natal territory by influencing the costs of dispersing and the benefits of delaying dispersal. I examined the influence of multiple factors on dispersal age in the banner-tailed kangaroo rat (Dipodomys spectabilis), a solitary species lacking extreme sex-biased dispersal. I used an information theoretic approach to compare Cox proportional hazards regression models of dispersal age for 121 offspring over a 3-year period consisting of low and high population densities. The top-ranked models indicated that dispersal age was influenced by a combination of socioecological factors related to resource competition, environmental conditions, kin competition, and a lesser extent sex. Circumstances that likely reduced the probability of successful dispersal such as intense resource competition at high population density and being born earlier in the breeding season when environmental conditions were poor lead to longer delays in natal dispersal. Offspring in larger litters also dispersed earlier possibly to avoid competition with kin. Sex was weakly supported in top models but may only influence dispersal age at high population densities. These results suggest that the proximal factors that trigger dispersal are influenced by a combination of multiple effects related to the costs of dispersing and the benefits of remaining at home, even in species that do not form long-term social groups or have extreme sex-biased dispersal.     

Components of lifetime reproductive success in communally and solitarily nursing house mice — a laboratory study

Under laboratory conditions, communal nursing among familiar and closely related female house mice (Mus domesticus) improved lifetime reproductive success compared to females rearing litters alone or females living with a previously unfamiliar, unrelated partner (reproductive success was measured within an experimental lifespan of 6 months, standardized as 120 days after mating at the age of about 2 months). An analysis of the contribution of three multiplicatively combined components to variation in reproductive success among breeding females revealed that, in all three social groups, survival of young until weaning contributed most to differences in lifetime reproduction (46–64% of the total variance). Females living with a sister had a significantly higher probability of reproducing successfully than females in the other groups, and also reared significantly more litters communally than females sharing nests with an unrelated partner. Weaning probabilities of young were highest in litters cared for by sisters and lowest in nests of unrelated females. Young were found dead either directly after birth (within the first 2 days of lactation) or after they had been cared for and nursed for at least 1 day. The loss of an entire litter typically occurred directly after birth. In monogamous females rearing litters alone the death of almost all young coincided with such early entire-litter mortality. In polygynous groups, however, offspring died at an older age and more litters suffered the loss of some young. Still, rearing young with a sister improved survival directly after birth and fewer litters were lost entirely in comparison with females in the other groups. In polygynous groups, pregnant females were observed to kill some of their partner's dependent young shortly before they gave birth themselves. As a consequence, individual young had reduced survival when they were firstborn in a communal nest (another litter was born within 16 days). Analyzed over a lifetime, communal care among familiar and closely related female house mice seems to be an adaptation to maximize the survival of offspring until weaning.     

Optimality of parental investment: The influence of nursing on reproductive success of mother and female young house mice

Summary The amount of parental milk investment determines not only the number of young the parent can produce, but also affects the offspring's fitness. The antagonism between quantity and quality of offspring was investigated in laboratory mice.In nursing first litters containing 2,4, ..., 14 pups, mothers invested increasing amounts of milk. This mainly extended the intervals between their first and second litters and slightly increased the size of their second litters, whilst third litters were not affected. In the female young, the decreasing amount each individual received as a result of increasing litter size led to delayed birth and reduced the size of their first litters. The intervals between their first and second litters and the size of the second litters were also affected, although to a lesser extent.Taking these results into consideration on a standard lifetime pattern of reproduction, the effects were calculated on net reproductive rates as an expression of fitness. Death rates were assumed that referred to population equilibrium or population growth. In both situations, the fitness curves of mothers and young showed that the actual level of milk investment and the level yielding optimal reproduction were in agreement. There was no significant deviation towards increased investment, as might result from parent-offspring conflict.     

Maternal nutrition affects offspring performance via maternal care in a subsocial spider

Provisioning of nutrients to the young during parental care is one of the mechanisms by which parents can affect growth and survival of their young and thus their reproductive success. We examined the hypothesis that food quality, i.e., ratio of macronutrients, provided to the young via maternal care affects their performance and the female’s reproductive success. The subsocial spider Stegodyphus lineatus exhibits intensive maternal care behaviors, including feeding the young and matriphagy (consumption of the mother). Our results showed that a protein-enriched diet resulted in larger females at maturation and higher survival of young, relative to intermediate or lipid-enriched diets. However, fecundity was not affected by female diet. We suggest that most of the nutrients are provided to the young during maternal care rather than deposited in the eggs, allowing females to economize on limited nutritional reserves. Females before maternal care showed a low protein and high lipid content relative to females before maturation and oviposition, suggesting a change in the nutritional requirement of females before maternal care. This change in macronutrient composition may be adaptive for the success of the young in the wild and shows a novel approach to animals’ ability to increase their reproductive success. Field-collected females showed a similar macronutrient composition as that of protein-enriched females in the lab, suggesting a high reproductive success of females in the wild. To our knowledge, this is the first time the importance of different macronutrients to females’ reproductive success is examined during reproduction.     

Aspects of population ecology in two populations of fiddler crabs, <Emphasis Type="Italic">Uca pugnax</Emphasis>

Fiddler crabs, Uca pugnax, were collected from a highly contaminated site and a relatively clean site, both in New Jersey to determine if and how environments with varying levels of pollutants may impact aspects of population biology including individual size, morphology (major cheliped size), population density, fecundity, recruitment and survivorship of early benthic phases. Crabs from the highly contaminated site were significantly larger in size, but had lower population density, lower recruitment, reduced reproductive season and lower survivorship of early benthic phases. Our study suggests that contamination may play a role in population ecology of U. pugnax. This study also determined that the reproductive season for U. pugnax in New Jersey is much longer than reported in the literature and could potentially be impacted by global climate change.     

Sexual selection and reproductive careers in mandrills (Mandrillus sphinx)

In sexually dimorphic, polygynous species, where males provide little parental care and competition between males for access to fertile females is high, sexual selection theory predicts sex differences in age-specific reproductive output and mortality profiles, and greater variance in lifetime reproductive success in males than in females. We examined age-specific reproductive output, mortality patterns and the extent and causes of variation in reproductive success for a semi-free-ranging colony of mandrills (Mandrillus sphinx, Cercopithecidae) in Franceville, Gabon, using long-term (20 year) demographic records and microsatellite parentage analysis. Although differences in the demography and feeding ecology of this closed, provisioned colony, in comparison with wild mandrills, limit interpretation of our results, sex differences in reproductive output and mortality showed the patterns predicted by sexual selection theory. Mortality was higher in males than in females after sexual maturity, and lifespan was significantly shorter in males (mean 14 year) than in females (>22 year). Age at first reproduction was significantly earlier in females (mean 4.2 year) than in males (11.6 year), and male reproductive output declined earlier. All females of breeding age produced offspring; while only 17 of 53 sexually mature males (32%) sired. Males sired a maximum of 41 offspring, versus 17 in females, and variance in male reproductive output was significantly greater than in females at all ages. The most important influence on variation in lifetime reproductive output in both sexes was joint variation between length of the breeding period and reproductive rate, due to lower reproductive rates in younger animals. Finally, social rank significantly influenced reproductive output in both sexes: high-ranking females began their reproductive careers earlier and had a higher subsequent reproductive rate than low-ranking females, while males that achieved top rank during their career sired far more offspring than males that did not.Electronic Supplementary Material Supplementary material is available for this article at     

Fitness costs of dispersal in red foxes (Vulpes vulpes)

The costs of dispersal are an important factor promoting natal philopatry, thereby encouraging the formation of social groups. The red fox, Vulpes vulpes, exhibits a highly flexible social system and one that is thought to represent a possible stage in the evolution of more complex patterns of group-living. Although the potential benefits accruing to philopatric offspring have previously been studied in this species, the potential costs of dispersal have received less attention. We contrasted survival rates, nutritional status, injuries and reproductive output of dispersing and non-dispersing male and female foxes in an urban population to assess the relative costs of dispersal versus natal philopatry. Mortality rates were not significantly higher for dispersing foxes, either in the short- or long-term. There was no evidence of increased nutritional stress in dispersing individuals. Dispersing individuals did, however, exhibit greater levels of wounding, although this did not appear to affect survival. Dispersing females were more likely to miss a breeding opportunity early in their reproductive lifespan. In contrast, both dispersing and non-dispersing males were unlikely to breed in their first year. We conclude that the major fitness component in females affected by dispersing is age at first reproduction.     

Interspecific hybridization in ants: at the intersection of ecology, evolution, and behavior

Ants are social and are haplodiploid. This combination may allow the evolution of a variety of unusual genetic pathways to achieve reproductive success. These include hybridizing across species, differential use of sperm to create a hybrid worker population, and reproductively isolated gene pools that depend on each other for their survival. Although there are demonstrable costs for colony development and reproduction, these phenomena may nevertheless be relatively common in nature. The specific ecological advantages that favor the evolution of these reproductive modes remain to be discovered.     

Resource allocation and population genetics of the bay scallop,Argopecten irradians irradians: effects of age and allozyme heterozygosity on reproductive output

The relationships among multiple-locus heterozygosity, age, reproduction and growth were examined over the ca. 2-yr lifespan of a cohort of northern bay scallops, Argopecten irradians irradians (Lamarck), from the Niantic River estuary, Connecticut, USA. Electrophoretic analyses revealed a relatively low proportion of polymorphic loci (=0.35) and low level of heterozygote deficiency ( D. across 6 loci=-0.05) in this population. Allele frequency distributions showed a high degree of temporal stability within and among cohorts. No significant correlation was found between multiple-locus heterozygosity and either somatic or reproductive growth. Our results lend support to the postulated linkage between low heterozygote deficit and lack of a heterozygosity/growth association in marine bivalves, and in the pectinid group in particular. Partial reproductive senility occurs in these scallops in their second year of life. Somatic tissue weight increased exponentially with increasing shell height, whereas pre-spawning gonad mass attained asymptotic values in 2-yr-old scallops. Thus, weight-specific reproductive effort was significantly lower in second- than first-year scallops (24 and 33% respectively). This pattern could be generated if high individual reproductive effort in the first year were correlated with accelerated (early) post-reproductive senescence. This kind of resource allocation, in which somatic growth is given precedence over reproductive growth in older individuals, has been previously reported in only one other bivalve, a pectinid (Chlamys islandica), in which the decline in reproductive effort occurs only after the scallops reach an age of ca. 20 yr.     

Old but gold: males preferentially cannibalize young eggs

Although counterintuitive at first sight, filial cannibalism is common in the animal kingdom and has been recognized as a mechanism to increase the cannibalizing parent’s lifetime reproductive success. However, previous evidence is often inconclusive and the adaptiveness of filial cannibalism is still not fully understood. We here address the notion that parents do not cannibalize at random but preferably consume offspring with a particular phenotype. To assess if differences in developmental stage and thus reproductive value of eggs trigger such selectivity, we experimentally presented male common gobies (Pomatoschistus microps) with two differently aged egg clutches within mixed broods. We found that males consumed significantly more young than old eggs. This result indicates that parents are not only able to discriminate between eggs based on developmental stage, but might use this to reduce the cost of partial filial cannibalism by selectively removing eggs of lower reproductive value.     

Fitness consequences of within-brood dominance in the cooperatively breeding acorn woodpecker

Social dominance confers potential advantages in terms of access to superior resources, habitats, and breeding opportunities. In the cooperatively breeding acorn woodpecker (Melanerpes formicivorus), within-brood dominance among juveniles is correlated with relative body size as nestlings. Capitalizing on this relationship, we investigated the fitness consequences of dominance by means of paired comparisons of broodmates. We found that (1) larger fledglings retained at least some of their size advantage as adults; (2) overwinter survival of larger, dominant fledglings was significantly greater than subordinates, but was not relatively greater when resources were poor than when they were good; (3) among birds surviving their first winter, there were no differences vis-à-vis dominance in terms of the proportion of birds acting as helpers or inheriting their natal territory. However, larger, dominant males were present in the study area longer than subordinates, suggesting that they either survived better or were more successful at gaining reproductive opportunities; (4) if only one male broodmate became a helper instead of dispersing, he was significantly more likely to be the smaller subordinate, consistent with the view that helping is a best-of-a-bad-job strategy; and (5) there were no significant differences in reproductive success among pairs of male broodmates that cobred together as adults, consistent with prior work failing to detect a phenotypic correlation of reproductive skew. Our results indicate that within-brood dominance relationships established as juveniles have significant effects on first-year survivorship and at least some aspects of adult fitness.     

Reproductive success in a low skew, communal breeding mammal: the banded mongoose, Mungos mungo

In most cooperatively breeding species, reproduction is monopolised by a subset of group members. However, in some species most or all individuals breed. The factors that affect reproductive success in such species are vital to understanding why multiple females breed. A key issue is whether or not the presence of other breeders is costly to an individual’s reproductive success. This study examines the factors that affect the post-parturition component of reproductive success in groups of communal-breeding banded mongoose (Mungos mungo), where up to ten females breed together. Per-litter reproductive success was low (only 18% of pups survived from birth to independence). Whilst singular breeding was wholly unsuccessful, there were costs associated with breeding in the presence of increasing numbers of other females and in large groups. Synchronisation of parturition increased litter success, probably because it minimises the opportunity for infanticide or decreases competitive asymmetry between pups born to different females. There was no evidence of inbreeding depression, and reproductive success was generally higher in litters where females only had access to related males within their group. I conclude that communal breeding in female banded mongooses represents a compromise between the benefits of group-living and communal pup care on the one hand, and competition between females to maximise their personal reproductive success on the other. Such conflicts are likely to occur in most communal breeding species. Whilst communal breeding systems are generally considered egalitarian, negative effects of co-breeders on individual reproductive success is still an issue.     

Calculating Ne and Ne/N in age-structured populations: a hybrid Felsenstein-Hill approach

The concept of effective population size (Ne) was developed under a discrete-generation model, but most species have overlapping generations. In the early 1970s, J. Felsenstein and W. G. Hill independently developed methods for calculating Ne in age-structured populations; the two approaches produce the same answer under certain conditions and have contrasting advantages and disadvantages. Here, we describe a hybrid approach that combines useful features of both. Like Felsenstein's model, the new method is based on age-specific survival and fertility rates and therefore can be directly applied to any species for which life table data are available. Like Hill, we relax the restrictive assumption in Felsenstein's model regarding random variance in reproductive success, which allows more general application. The basic principle underlying the new method is that age structure stratifies a population into winners and losers in the game of life: individuals that live longer have more opportunities to reproduce and therefore have a higher mean lifetime reproductive success. This creates different classes of individuals within the population, and grouping individuals by age at death provides a simple means of calculating lifetime variance in reproductive success of a newborn cohort. The new method has the following features: (1) it can accommodate unequal sex ratio and sex-specific vital rates and overdispersed variance in reproductive success; (2) it can calculate effective size in species that change sex during their lifetime; (3) it can calculate Ne and the ratio Ne/N based on various ways of defining N; (4) it allows one to explore the relationship between Ne and the effective number of breeders per year (Nb), which is a quantity that genetic estimators of contemporary Ne commonly provide information about; and (5) it is implemented in freely available software (AgeNe).     

The role of life histories and trophic interactions in population recovery

Factors affecting population recovery from depletion are at the focus of wildlife management. Particularly, it has been debated how life‐history characteristics might affect population recovery ability and productivity. Many exploited fish stocks have shown temporal changes towards earlier maturation and reduced adult body size, potentially owing to evolutionary responses to fishing. Whereas such life‐history changes have been widely documented, their potential role on stock's ability to recover from exploitation often remains ignored by traditional fisheries management. We used a marine ecosystem model parameterized for Southeastern Australian ecosystem to explore how changes towards “faster” life histories might affect population per capita growth rate r. We show that for most species changes towards earlier maturation during fishing have a negative effect (3–40% decrease) on r during the recovery phase. Faster juvenile growth and earlier maturation were beneficial early in life, but smaller adult body sizes reduced the lifetime reproductive output and increased adult natural mortality. However, both at intra‐ and inter‐specific level natural mortality and trophic position of the species were as important in determining r as species longevity and age of maturation, suggesting that r cannot be predicted from life‐history traits alone. Our study highlights that factors affecting population recovery ability and productivity should be explored in a multi‐species context, where both age‐specific fecundity and survival schedules are addressed simultaneously. It also suggests that contemporary life‐history changes in harvested species are unlikely to increase their resilience and recovery ability.