An official website of the United States government
Abstract Exploring age‐ and sex‐specific survival rates provides insight regarding population behavior and life‐history trait evolution. However, our understanding of how age‐specific patterns of survival, including actuarial senescence, compare between the sexes remains inadequate. Using 36 years of mark‐recapture data for 7,516 male Weddell seals (Leptonychotes weddellii) born in Erebus Bay, Antarctica, we estimated age‐specific annual survival rates using a hierarchical model for mark‐recapture data in a Bayesian framework. Our male survival estimates were moderate for pups and yearlings, highest for 2‐year‐olds, and gradually declined with age thereafter such that the oldest animals observed had the lowest rates of any age. Reports of senescence in other wildlife populations of species with similar longevity occurred at older ages than those presented here. When compared to recently published estimates for reproductive Weddell seal females, we found that peak survival rates were similar (males: 0.94, 95% CI = 0.92–0.96; females: 0.92, 95% CI = 0.93–0.95), but survival rates at older ages were lower in males. Age‐specific male Weddell seal survival rates varied across years and individuals, with greater variation occurring across years. Similar studies on a broad range of species are needed to contextualize these results for a better understanding of the variation in senescence patterns between the sexes of the same species, but our study adds information for a marine mammal species to a research topic dominated by avian and ungulate species.
more »
« less
This content will become publicly available on January 16, 2026
A comparison of sex-specific senescence patterns in a long-lived marine mammal
The lifetime fitness of an individual is determined by the integrated results of survival and reproduction. Improving our understanding of variation in survival senescence within and between species will therefore provide greater insight into the evolution of different life history strategies. Survival is influenced by multiple factors, consequently, variation in patterns of senescence is expected between individuals and sexes and across mating systems and the continuum of life history strategies. To date there is little consensus regarding the mechanisms driving the evolution of sex differences in actuarial senescence, necessitating the need for studies of sex-specific senescence for species across a wide range of life histories. The Weddell seal is a species of long-lived mammal that displays moderate polygyny and little sexual size dimorphism, which makes it an unusual species compared to other long-lived mammals that share the polygynous mating system. Here we used 37 years of data for 1,879 female and 1,474 male Weddell seals from Erebus Bay, Antarctica, to estimate and compare sex-specific patterns of survival rates using basis splines which allow flexible modeling of age-specific patterns. We found that males had lower rates of survival throughout life and higher rates of actuarial senescence after early adulthood compared to females. These results add to our understanding of sex-specific survival rates in the species and contribute information for a long-lived, polygynous species that should aid in achieving a broader understanding of aging between sexes and across the tree of life.
more »
« less
- PAR ID:
- 10593023
- Editor(s):
- Gray, David A
- Publisher / Repository:
- Nature Publishing Group
- Date Published:
- Journal Name:
- Frontiers in Ecology and Evolution
- Volume:
- 12
- ISSN:
- 2296-701X
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
More Like this
-
-
Abstract Parental care, mating dynamics and life history co‐evolve. Understanding the diversity of reproductive patterns found in nature is a major focus of evolutionary ecology research. Previous research suggests that the origin of parental care of eggs will be favoured when egg and adult death rates and juvenile survival are relatively high. However, the previous research that explored the link between care and life history did not account for among‐species variation in mating dynamics. As mating dynamics are generally expected to influence care, we explore, theoretically, the life‐history conditions (stage‐specific rates of maturation and survival) that favour parental care across three mating scenarios: reproductive rate (1) is unaffected by males (assuming that some males are present), (2) increases as male abundance increases or (3) decreases as male abundance increases. Across scenarios, all forms of care were most strongly favoured when egg and adult death rates, juvenile survival and female egg maturation rates were relatively high. When reproductive rate was unaffected by male abundance or increased as male abundance increased, as we might expect in systems in which females are mate‐limited, all forms of care were most strongly favoured when male egg maturation rate (i.e. the rate at which male eggs develop, mature and hatch) was moderate or high. When greater male abundance inhibited reproduction, which might occur in systems with intense male–male competition, all forms of care were most strongly favoured when male egg maturation rate was low‐to‐moderate. These results suggest that life history affects the evolution of parental care, and sex‐specific life history can interact with mating dynamics to influence the origin of care.more » « less
-
Abstract Sex‐related differences in vital rates that drive population change reflect the basic life history of a species. However, for visually monomorphic bird species, determining the effect of sex on demographics can be a challenge. In this study, we investigated the effect of sex on apparent survival, recruitment, and breeding propensity in the Adélie penguin (Pygoscelis adeliae), a monochromatic, slightly size dimorphic species with known age, known sex, and known breeding history data collected during 1996–2019 (n = 2127 birds) from three breeding colonies on Ross Island, Antarctica. Using a multistate capture–mark–recapture maximum‐likelihood model, we estimated apparent survival (), recapture (resighting) probability (), and the probability of transitioning among breeding states and moving between colonies (; colony‐specific non‐juvenile pre‐breeders, breeders, and non‐breeders). Survival rate varied by breeding status and colony, but not sex, and pre‐breeders had higher survival rates than breeders and non‐breeders. Females had a higher probability of recruiting into the breeding population each year and may enter the breeding pool at younger ages. In contrast, both sexes had the same probability of breeding from year to year once they had recruited. Although we detected no direct sex effects on survival, the variation in recruitment probability and age‐at‐first reproduction, along with lower survival rates of breeders compared to pre‐breeders, likely leads to shorter lifespans for females. This is supported by our findings of a male‐biased mean adult sex ratio (ASR) of 1.4 males for every female ( proportion of males = 0.57, SD = 0.07) across all colonies and years in this metapopulation. Our study illustrates how important it can be to disentangle sex‐related variation in population vital rates, particularly for species with complex life histories and demographic dynamics.more » « less
-
Abstract Females and males can exhibit striking differences in body size, relative trait size, physiology, and behavior. As a consequence, the sexes can have very different rates of whole-body energy use, or converge on similar rates through different physiological mechanisms. Yet many studies that measure the relationship between metabolic rate and body size only pay attention to a single sex (more often males), or do not distinguish between sexes. We present four reasons why explicit attention to energy-use between the sexes can yield insight into the physiological mechanisms that shape broader patterns of metabolic scaling in nature. First, the sexes often differ considerably in their relative investment in reproduction, which shapes much of life-history and rates of energy use. Second, males and females share a majority of their genome but may experience different selective pressures. Sex-specific energy profiles can reveal how the energetic needs of individuals are met despite the challenge of within-species genetic constraints. Third, sexual selection often pushes growth and behavior to physiological extremes. Exaggerated sexually selected traits are often most prominent in one sex, can comprise up to 50% of body mass, and thus provide opportunities to uncover energetic constraints of trait growth and maintenance. Finally, sex-differences in behavior such as mating-displays, long-distance dispersal, and courtship can lead to drastically different energy allocation among the sexes; the physiology to support this behavior can shape patterns of metabolic scaling. The mechanisms underlying metabolic scaling in females, males, and hermaphroditic animals can provide opportunities to develop testable predictions that enhance our understanding of energetic scaling patterns in nature.more » « less
-
Abstract Both tree size and life history variation drive forest structure and dynamics, but little is known about how life history frequency changes with size. We used a scaling framework to quantify ontogenetic size variation and assessed patterns of abundance, richness, productivity and light interception across life history strategies from >114,000 trees in a primary, neotropical forest. We classified trees along two life history axes: afast–slowaxis characterized by a growth–survival trade‐off, and astature–recruitmentaxis with tall,long‐lived pioneersat one end and short,short‐lived recruitersat the other.Relative abundance, richness, productivity and light interception follow an approximate power law, systematically shifting over an order of magnitude with tree size.Slowsaplings dominate the understorey, butslowtrees decline to parity with rapidly growingfastandlong‐lived pioneerspecies in the canopy.Like the community as a whole,slowspecies are the closest to obeying the energy equivalence rule (EER)—with equal productivity per size class—but other life histories strongly increase productivity with tree size. Productivity is fuelled by resources, and the scaling of light interception corresponds to the scaling of productivity across life history strategies, withslowandallspecies near solar energy equivalence. This points towards a resource‐use corollary to the EER: the resource equivalence rule.Fitness trade‐offs associated with tree size and life history may promote coexistence in tropical forests by limiting niche overlap and reducing fitness differences.Synthesis. Tree life history strategies describe the different ways trees grow, survive and recruit in the understorey. We show that the proportion of trees with a pioneer life history strategy increases steadily with tree size, as pioneers become relatively more abundant, productive, diverse and capture more resources towards the canopy. Fitness trade‐offs associated with size and life history strategy offer a mechanism for coexistence in tropical forests.more » « less
