The role of menopause and reproductive senescence in a long-lived social mammal
© Ward et al; licensee BioMed Central Ltd. 2009
Received: 04 June 2008
Accepted: 03 February 2009
Published: 03 February 2009
Menopause is a seemingly maladaptive life-history trait that is found in many long-lived mammals. There are two competing evolutionary hypotheses for this phenomenon; in the adaptive view of menopause, the cessation of reproduction may increase the fitness of older females; in the non-adaptive view, menopause may be explained by physiological deterioration with age. The decline and eventual cessation of reproduction has been documented in a number of mammalian species, however the evolutionary cause of this trait is unknown.
We examined a unique 30-year time series of killer whales, tracking the reproductive performance of individuals through time. Killer whales are extremely long-lived, and may have the longest documented post-reproductive lifespan of any mammal, including humans. We found no strong support for either of the adaptive hypotheses of menopause; there was little support for the presence of post-reproductive females benefitting their daughter's reproductive performance (interbirth interval and reproductive lifespan of daughters), or the number of mature recruits to the population. Oldest mothers (> 35) did appear to have a small positive impact on calf survival, suggesting that females may gain experience with age. There was mixed support for the grandmother hypothesis – grandoffspring survival probabilities were not influenced by living grandmothers, but grandmothers may positively influence survival of juveniles at a critical life stage.
Although existing data do not allow us to examine evolutionary tradeoffs between survival and reproduction for this species, we were able to examine the effect of maternal age on offspring survival. Our results are consistent with similar studies of other mammals – oldest mothers appear to be better mothers, producing calves with higher survival rates. Studies of juvenile survival in humans have reported positive benefits of grandmothers on newly weaned infants; our results indicate that 3-year old killer whales may experience a positive benefit from helpful grandmothers. While our research provides little support for menopause evolving to provide fitness benefits to mothers or grandmothers, our work supports previous research showing that menopause and long post-reproductive lifespans are not a human phenomenon.
Individuals in many mammalian species devote a fraction of their lives to reproduction. Females in these species experience a gradual midlife decline in reproductive performance with age, and eventually menopause, the abrupt termination of reproduction . In contrast, males are typically able to reproduce until old age, with only a slight decrease in reproductive ability. Although anthropologists have suggested that menopause is unique to primates  or even just humans [3, 4], the phenomenon appears to be widespread in mammals – in a meta-analysis of 42 species, Cohen (2004) found support for post-reproductive lifespans (PRLS) in 83% of taxa. More recent studies have shown that there are a range of species with relatively little or no parental investment that also exhibit reproductive senescence and cessation, including species generally considered to be 'r-selected'. These species include guppies , parakeets , mice , and beetles .
Although reproductive senescence or menopause may be relatively common, only a handful of species have extremely long post-reproductive lifespans. Why do females of some species live so long after reproduction ceases? On the surface, this would appear to be a maladaptive life-history trait. Several hypotheses, adaptive and non-adaptive, have been proposed to explain the evolutionary significance of menopause.
The attentive mother hypothesis
Under the adaptive view of menopause, the cessation of reproduction allows for an increase in individual or inclusive fitness . This so-called "attentive mother" hypothesis predicts that as the level of required infant care increases, early reproductive termination allows females to provide a marginal benefit to the survival of existing offspring . Older females that stop reproducing simultaneously avoid risky pregnancies. Of all primate species, evidence supporting the attentive mother hypothesis is limited to humans . A variant of this theory, also only applicable to primates, is the "altriciality-lifespan" model. This hypothesis correlates brain size with parental care, suggesting that an increase in the age at the onset of menopause may be coupled with selection for long lifespans .
The helpful grandmother hypothesis
A second adaptive theory of menopause is the grandmother hypothesis. By extending their lifespans after reproduction ceases, post-reproductive females who help daughters or other kin raise offspring increase their own inclusive fitness [10, 11]. Specifically, females with living mothers may experience increased fecundity rates, decreased interbirth intervals (IBI), and increased reproductive lifespans [12, 13]. Evidence supporting the grandmother hypothesis is inconclusive, and limited to humans. In a study of 18th century humans, Lahdenpera et al. (2004) showed a positive effect of grandmothers on both grandchild survival to maturity and the reproductive lifespan of daughters. Additional studies of the grandmother hypothesis have failed to find support in other social species, including lions and baboons , macaques , and pre-industrial humans [15, 16]. The lack of support for the grandmother hypothesis may be due to a lack of high quality longitudinal data, contradictory effects of maternal and paternal grandmothers , or complicated kin relationships .
The mutation accumulation hypothesis
An alternative hypothesis to the adaptive views of menopause is the "mutation accumulation" model [9, 19]. Under this hypothesis, senescence is a result of physiological deterioration associated with aging, and weak selection on aged individuals due to few animals living to extremely old ages. Menopause becomes a byproduct of this process, and is more evident when selection acts to increase longetivity, increasing the difference between the lifespans of the reproductive and somatic systems . Support for the mutation accumulation hypothesis is generally indirect, consisting of rejecting competing hypotheses [12, 21].
Reproductive senescence and menopause in killer whales
One of the reasons that killer whales have been thought to support the grandmother hypothesis is that their social structure is matrilineal. Collections of matrilines – a mother and her offspring – associate with other matrilines, forming larger social aggregations of related individuals ('groups' or 'pods'). Among piscivorous killer whales (also known as 'residents'), males and females are both philopatric and remain with their natal matriline throughout their life (fathers contribute no parental care). From a kin-selection perspective, individuals in the same matriline engage in many of the same food sharing behaviors that have been linked to the grandmother hypothesis in human populations [10, 31]. While it is not possible to quantify the benefit of food sharing for this species, additional mechanisms that may enable grandmothers to increase inclusive fitness may be providing additional care for newborns, or benefitting the social unit by retaining cultural information such as knowledge of historically good hunting areas [32, 33].
The length of killer whale post-reproductive lifespans has led some authors to suggest that the grandmother hypothesis is responsible for the extreme longevity of females in this species , however support for the grandmother hypothesis has not been evaluated with data. The aim of this study was to quantify the data support for both adaptive views of menopause using long-term data tracking every individual killer whale. We used these data to estimate the effect of post-reproductive mothers and grandmothers on demographic rates, using data collected from two distinct populations of killer whales. First, we examined whether maternal covariates had positive effects on the survival of offspring. As a long lived species, there may be a tradeoff in the energy that female killer whales devote to survival and reproduction ; females that devote more energy toward reproduction may experience higher mortality later in life [35, 36]. Second, we evaluated support for the grandmother hypothesis – specifically, whether post-reproductive females had positive effects on the survival of grandoffspring, the reproductive lifespan of their daughters, or the time interval between their daughters' births. Finally, we evaluated whether there were sufficient data to estimate maternal tradeoffs between survival and reproduction.
Longitudinal sightings data were collected from two neighboring populations of fish-eating killer whales over the last 30 years, 1978–2007 [23, 37, 38]: the Northern and Southern Resident killer whales which inhabit the inland and nearshore waters of Washington state (USA) and British Columbia (Canada). These populations are discrete; they do not interbreed, and neither immigration nor emigration have been observed . During annual photographic surveys, nearly every individual in the population has been recorded. Each individual has unique pigmentation, scars, and fin shapes, allowing us to track the survival and reproductive performance of each female over time. Although detailed age and birth data do exist for recent years, information on birth defects, still births, or mortality risk to pregnant females is not available. Due to low adult mortality , the majority of females in our study are expected to live beyond the onset of menopause.
To evaluate support for the attentive mother hypothesis, we examined whether covariate attributes of mothers (age, dead/alive, birth order) had any impact on the survival of calves (ages 0 to 1) or on juvenile survival (< age 5) for individuals born since 1978. Binomial generalized linear models (GLMs) with a logit link were used to model survival (φ) as a function of covariates, e.g. . The Schwarz criterion or BIC  was calculated for each competing model, and differences between BIC values were used as an approximation to the Bayes factor . If there are two competing models, the approximate Bayes factor supporting model 1 over model 2 is BF12 = exp [-(BIC1 - BIC2)/2]. When two models are considered, this formula allows the posterior probability of each model given the data to be computed, Pr [M1|Y] = BF12/(1+BF12), because the Bayes factor can also be viewed as the ratio of the posterior model probabilities.
To examine support for the grandmother hypothesis, we first looked at impacts of grandmothers on their daughters, and second evaluated potential impacts of grandmothers on grandoffspring survival. The reproductive lifespan of mature females was modeled using GLMs to evaluate support for including mothers' survival status as a covariate. Because the precise onset of reproductive termination cannot be determined, we defined the response variable (reproductive lifespan) as the number of years between the last and first birth. Only females whose mothers' survival status did not change over their reproductive histories were included in this calculation. An alternative effect grandmothers may have is that by providing additional care, daughters may be more productive (shortening the time between births). To examine support for this hypothesis, we constructed a model of interbirth intervals (IBI) as the response variable. The survival status of each females' mother (alive/dead) was included as a covariate to evaluate whether females with alive mothers had a shorter IBI compared to females with dead mothers. As the second component of evaluating the grandmother hypothesis, we expanded GLMs of survival to include the grandmothers' survival status as a covariate – in these models, we compared the age-specific survival rates of juveniles with living grandmothers to those with dead grandmothers. Two analyses were performed; in the first case we examined the impact of grandmothers on survival of calves (aged 0 to 1), in the second we examined this factor across juveniles (aged < 5).
One hypothesis for why survival of primiparous calves may be relatively low is that older mothers may be more experienced than younger mothers [41, 42]. An alternative hypothesis is that there may be an evolutionary tradeoff between current survival and future reproduction – young females may prioritize their own survival above that of potential offspring, delaying reproduction . To evaluate evidence supporting this hypothesis, we first had to quantify lifetime reproductive success (LRS) for each female. Several different approaches have been used to measure LRS. Lahdenpera et al. (2004) used the number of births as a response variable, however using the raw number of births has been criticized because it doesn't account for survival to maturity . A second approach is to calculate the individual growth rate, λ  – this method has only been applied to short-lived species and cannot be applied to right-censored data, such as that in our study. A third approach involves estimating total recruits to the population, R0 . This latter method may be more robust than calculating the individual λ because it is considered rate-insensitive .
Support for the mutation accumulation hypothesis
Evolutionary theory predicts that if menopause is simply a byproduct of senescence, the difference between female lifespan and menopause would be approximately equal to the time necessary for a female to live long enough to raise her last offspring . Killer whale fecundity declines gradually after age 23, and rapidly after age 40 (reproduction ceases by age 45) [22, 26]. The difference between mean female life expectancy (55.1) and age at reproductive cessation (45) is approximately the same as the age at female maturity . This result may be spurious if reproductive cessation results from the mutation accumulation or attentive mother hypotheses, but it also suggests that killer whale mothers may be similar to humans in that weaned juveniles may continue to be somewhat dependent on the presence of their mother, at least until they reach reproductive maturity.
Support for the attentive mother hypothesis
Models of calf and juvenile survival.
Pr [M|Y] v. null
Pr [M|Y] v. null
age + age2
moms > 35 (F)
first born (F)
Support for the grandmother hypothesis
GLM models illustrating how other hypotheses about killer whale reproduction were evaluated.
mom's survival status
mom's survival status
grandma's survival status
grandma's survival status + maternal age
Tradeoffs between survival and reproduction
Over all simulations, the distribution of the regression coefficient relating age at maturity to LRS was slightly positive (Fig. 3d), however the large variance prevents any conclusive inference about the relationship between age at maturity and reproduction (specifically, whether mothers that delay reproduction produce more viable calves later in life). Although three types of uncertainty were included in these projections, virtually no uncertainty existed in future survival of adult females (φ~0.99), and the largest source of variability was age-specific natality over ages 25–45 . As these older animals reach menopause over the next 20 years, their reproductive performance will continue to provide more information about potential tradeoffs between age at maturity and lifetime reproductive success.
Hamilton (1966) first posited the idea of the "wall of death" – the idea that once females cease reproduction, mortality should increase rapidly as there is not selection pressure for continued survival . We know that in human populations, there is little support for the "wall of death" hypothesis, even in hunter-gather populations where one cannot make the argument that survival past reproduction is due to artificially extended lifespan . Until recently, it has been argued that menopause is specific to primates and that the "wall of death" still applies to non-primates. However, biologists have shown that menopause is a much more prevalent life-history trait in non-primates than was previously supposed [12, 29]. As we show in this study, killer whales show even less support for the "wall of death" idea than human hunter-gatherer populations . In these hunter-gatherer populations, approximately 30% of human females lived past reproduction; in contrast, more than 50% of killer whale females are expected to live beyond the onset of menopause (Fig. 1) [22, 26].
Although there is some debate in the literature, we follow Cohen  and lump the attentive mother hypothesis and the helpful grandmother hypothesis into adaptive hypotheses for menopause. One explanation for the long post-reproductive lifespans that have been observed in killer whales is the presence (and potential helpfulness) of older matriarchal females within matrilineal units . Using multiple modeling approaches, we found limited support for either of these adaptive explanations of menopause.
If the attentive mother hypothesis alone was responsible for the cessation of reproduction in killer whales, we would expect females to live just long enough to raise their last offspring to independence (2–3 years, to age 42–43). On average, female killer whales appear to live an average of 7–8 years longer than this (> 50 years, ) – roughly equivalent to the time needed for offspring to reach reproductive maturity. There is some uncertainty in the estimated life expectancy beyond menopause, however, due to the small sample size used and uncertainty in some ages of the oldest individuals . For the attentive mother hypothesis to be responsible for menopause in killer whales, several biological conditions must be met: the probability of older females giving birth must decline with age, offspring born prior to the cessation of reproduction must experience some benefit, and the rates of birth defects, stillbirths and maternal mortality may increase with maternal age . While the first two conditions appear to be met for this species ( and this study, respectively), data on stillbirths, birth defects, and maternal mortality do not exist. While it is unlikely that this data will be collected on killer whales or other free-ranging marine mammals, this question may be best explored in future research on terrestrial mammals with relatively long post-reproductive lifespans.
Although not directly related to the attentive mother hypothesis, we found that the oldest mothers may also be the best mothers – calves born to females approaching menopause had higher estimated survival rates than calves of younger mothers. These older females may be more successful in raising young because of maternal experience, or they may allocate more effort to reproduction relative to younger females. This same result did not hold when older females were used to model juvenile survival, suggesting that older mothers may be more experienced in caring for calves during their most dependent period (ages 0–1). After weaning, juveniles may depend on additional benefits from related individuals – fathers provide little to no parental care in this species, but older siblings or related adult females may contribute in raising young.
If the grandmother hypothesis was responsible for the cessation of reproduction in killer whales, either daughters or grandoffspring would be expected to benefit from the presence of post-reproductive females. From the perspective of the grandmother's fitness, the difference between these responses amounts to a tradeoff between the quantity and quality of grandoffspring produced. Post-reproductive females did not appear to have an effect on the number of calves produced by their daughters (either a shorter interbirth interval, longer reproductive lifespan or increased calving probability). Post-reproductive females also did not appear to benefit newborn grandoffspring, but following other studies, one of the age groups that may receive the largest benefit are newly weaned animals. In human studies, grandmothers have been shown to be one of the most common forms of kin selection . An analysis of human menopause in 20th century Gambia suggested that the benefit of grandmothers may occur during an extremely small temporal window, immediately after grandchildren are not completely dependent on their mothers . The most compelling evidence supporting a positive benefit of killer whale grandmothers is the survival of grandoffspring between their 2nd and 3rd birthdays (Fig. 4). While including the survival status of grandmothers is not supported across all age classes, the posterior probability of the grandmother effect increases when only 2 year olds are included, but is still approximately equal to 50:50 support (Pr [M|Y] = 0.48 versus 0.05).
In a review of current evidence for post-reproductive lifespans in multiple taxa, Cohen's  non-adaptive hypothesis for the evolution of menopause suggests that there may be two forms of selection acting separately on reproductive and somatic lifespans. Cohen's hypothesis may explain the phenomenon of long post-reproductive lifespans in killer whales, but cannot be evaluated with existing data. To test this hypothesis using the longitudinal data in our study, we would need to examine whether total lifespans are uncorrelated with the length of reproductive lifespans . Due to the extreme longevity of this species, females that were reaching reproductive maturity at the beginning of this study are currently reaching menopause, and are expected to live for another 15 years.
In summary, like other studies of long-lived mammals [12, 29], we found weak support for both of the adaptive hypotheses for menopause. Perhaps for anthropogenic reasons, the attentive mother and helpful grandmother hypotheses seem natural explanations for the presence of old females in social species – especially species that form multi-generation matriarchal groups. Aside from weak evidence in human populations, multiple studies have failed to find strong support for either of these adaptive hypotheses in other mammals. This does not mean that the hypothesis of "social transfer"  (the cultural transmission of knowledge and skills) or coalition formation  does not play a part in the evolution of menopause or the presence of old females in social groups. Rather, it suggests that if social transfers are playing a role, it is through more subtle effects than simply increasing the survival of daughters and granddaughters.
Long-term demographic data for resident killer whales were provided by the Center for Whale Research and Fisheries and Oceans Canada. Funding supporting EW was provided by a post-doctoral research fellowship from the National Research Council. M. Ford offered suggestions that improved the quality of the manuscript.
- Pavelka MSM, Fedigan LM, Zohar S: Availability and adaptive value of reproductive and post-reproductive Japanese macaque mothers and grandmothers. Animal Behaviour. 2002, 64: 407-414. 10.1006/anbe.2002.3085.View ArticleGoogle Scholar
- Alvarez HP: Grandmother hypothesis and primate life histories. American Journal of Physical Anthropology. 2000, 113: 435-450. 10.1002/1096-8644(200011)113:3<435::AID-AJPA11>3.0.CO;2-O.View ArticlePubMedGoogle Scholar
- Peccei JS: A Hypothesis for the Origin and Evolution of Menopause. Maturitas. 1995, 21: 83-89. 10.1016/0378-5122(94)00884-A.View ArticlePubMedGoogle Scholar
- Shanley DP, Kirkwood TBL: Evolution of the human menopause. Bioessays. 2001, 23: 282-287. 10.1002/1521-1878(200103)23:3<282::AID-BIES1038>3.0.CO;2-9.View ArticlePubMedGoogle Scholar
- Reznick D, Bryant M, Holmes D: The evolution of senescence and post-reproductive lifespan in guppies (Poecilia reticulata). Plos Biology. 2006, 4: 136-143. 10.1371/journal.pbio.0040007.View ArticleGoogle Scholar
- Holmes DJ, Ottinger MA: Birds as long-lived animal models for the study of aging. Experimental Gerontology. 2003, 38: 1365-1375. 10.1016/j.exger.2003.10.018.View ArticlePubMedGoogle Scholar
- Nelson JFLSF: Reproductive aging in the female: an etiological perspective. Review of Biological Research in Aging. 1985, 2: 251-314.Google Scholar
- Omkar , Singh SK, Singh K: Effect of age on reproductive attributes of an aphidophagous ladybird, Cheilomenes sexmaculata. Insect Science. 2006, 13: 301-308. 10.1111/j.1744-7917.2006.00098.x.View ArticleGoogle Scholar
- Williams GC: Pleiotropy, natural selection and the evolution of senescence. Evolution. 1957, 22: 406-421.Google Scholar
- Hawkes K, O'Connell JF, Jones NGB, Alvarez H, Charnov EL: Grandmothering, menopause, and the evolution of human life histories. Proceedings of the National Academy of Sciences of the United States of America. 1998, 95: 1336-1339. 10.1073/pnas.95.3.1336.PubMed CentralView ArticlePubMedGoogle Scholar
- Foster KR, Ratnieks FLW: A new eusocial vertebrate?. Trends in Ecology & Evolution. 2005, 20: 363-364. 10.1016/j.tree.2005.05.005.View ArticleGoogle Scholar
- Packer C, Tatar M, Collins A: Reproductive cessation in female mammals. Nature. 1998, 392: 807-811. 10.1038/33910.View ArticlePubMedGoogle Scholar
- Lahdenpera M, Lummaa V, Helle S, Tremblay M, Russell AF: Fitness benefits of prolonged post-reproductive lifespan in women. Nature. 2004, 428: 178-181. 10.1038/nature02367.View ArticlePubMedGoogle Scholar
- Fedigan LM, Pavelka MSM: Is there adaptive value to reproductive termination in Japanese macaques? A test of maternal investment hypotheses. International Journal of Primatology. 2001, 22: 109-125. 10.1023/A:1005618312088.View ArticleGoogle Scholar
- Hill K, Hurtado AM: The evolution of reproductive senescence and menopause in human females. Human Nature. 1991, 2: 315-350. 10.1007/BF02692196.View ArticleGoogle Scholar
- Rogers A: Why menopause?. Evolutionary Ecology. 1993, 7: 406-420. 10.1007/BF01237872.View ArticleGoogle Scholar
- Voland E, Beise J: Opposite effects of maternal and paternal grandmothers on infant survival in historical Krummhorn. Behavioral Ecology and Sociobiology. 2002, 52: 435-443. 10.1007/s00265-002-0539-2.View ArticleGoogle Scholar
- Hawkes K, O'Connell JF, Blurton Jones NG, Gurven M, Hill K, Hames R, Kano T, Nishida T, White FJ, Churchill SE, Worthman CM: Hadza women's time allocation, offspring provisioning, and the evolution of long postmenopausal life spans. Current Anthropology. 1997, 38: 551-577. 10.1086/204646.View ArticleGoogle Scholar
- Hamilton WD: The moulding of senescence by natural selection. Journal of Theoretical Biology. 1966, 12: 12-45. 10.1016/0022-5193(66)90184-6.View ArticlePubMedGoogle Scholar
- Peccei JS: A critique of the grandmother hypotheses: Old and new. American Journal of Human Biology. 2001, 13: 434-452. 10.1002/ajhb.1076.View ArticlePubMedGoogle Scholar
- Bowen WD, Iverson SJ, McMillan JI, Boness DJ: Reproductive performance in grey seals: age-related improvement and senescence in a capital breeder. Journal of Animal Ecology. 2006, 75: 1340-1351. 10.1111/j.1365-2656.2006.01157.x.View ArticlePubMedGoogle Scholar
- Olesiuk PF, Bigg MA, Ellis GM: Life History and Population Dynamics of Resident Killer Whales (Orcinus orca) in the Coastal Waters of British Columbia and Washington State. Report of the International Whaling Commission. 1990, 12: 209-243.Google Scholar
- Center for Whale Research: Southern Resident Killer Whale ID Guide. 2007, Friday Harbor, WA: Center for Whale ResearchGoogle Scholar
- Bigg MA, Olesiuk PF, Ellis GM, Ford JKB, Balcomb KC: Social organizations and genealogy of resident killer whales (Orcinus orca) in the coastal waters of British Columbia and Washington State. Report of the International Whaling Commission. 1990, 383-405. Special Issue 12
- Howell N: Demography of the Dobe !Kung. 1979, New York: Academic PressGoogle Scholar
- Ward EJ, Holmes EE, Balcomb KC: Evidence of reproductive senescence and prey limitation in killer whales. In review, Journal of Applied Ecology. 2008Google Scholar
- Foote AD: Mortality rate acceleration and post-reproductive lifespan in matrilineal whale species. Biology Letters. 2008, 4: 189-191. 10.1098/rsbl.2008.0006.PubMed CentralView ArticlePubMedGoogle Scholar
- Moss CJ: The demography of an African elephant (Loxodonta africana) population in Amboseli, Kenya. Journal of Zoology. 2001, 255: 145-156. 10.1017/S0952836901001212.View ArticleGoogle Scholar
- Cohen AA: Female post-reproductive lifespan: a general mammalian trait. Biological Reviews. 2004, 79: 733-750. 10.1017/S1464793103006432.View ArticlePubMedGoogle Scholar
- Kaplan H, Hill K, Lancaster J, Hurtado AM: A theory of human life history evolution: diet, intelligence and longetivity. Evolutionary Anthropology. 2000, 9: 156-185. 10.1002/1520-6505(2000)9:4<156::AID-EVAN5>3.0.CO;2-7.View ArticleGoogle Scholar
- Ford JKB, Ellis GM: Selective foraging by fish-eating killer whales Orcinus orca in British Columbia. Marine Ecology Progress Series. 2006, 316: 185-199. 10.3354/meps316185.View ArticleGoogle Scholar
- Konig B: Cooperative care of young in mammals. Naturwissenschaften. 1997, 84: 95-104. 10.1007/s001140050356.View ArticlePubMedGoogle Scholar
- McAuliffe K, Whitehead H: Eusociality, menopause and information in matrilineal whales. Trends in Ecology & Evolution. 2005, 20: 650-650. 10.1016/j.tree.2005.09.003.View ArticleGoogle Scholar
- Kirkwood TBL, Rose MR: Evolution of Senescence – Late Survival Sacrificed for Reproduction. Philosophical Transactions of the Royal Society of London Series B-Biological Sciences. 1991, 332: 15-24. 10.1098/rstb.1991.0028.View ArticleGoogle Scholar
- Reznick D: Costs of reproduction: an evaluation of the empirical evidence. Oikos. 1985, 44: 257-267. 10.2307/3544698.View ArticleGoogle Scholar
- Roff DA: The Evolution of Life Histories: Theory and Analysis. 1992, London: Chapman and HallGoogle Scholar
- Ellis GM, Ford JKB, Towers JR: Northern Resident Killer Whales in British Columbia: Photo-Identification Catalog. 2007, Canada DFO, NanaimoGoogle Scholar
- Ford JKB, Ellis GM, Balcomb KC: Killer Whales: The Natural History and Genealogy of Orcinus Orca and Washington State. 2000, Seattle: University of Washington PressGoogle Scholar
- Schwarz G: Estimating Dimension of a Model. Annals of Statistics. 1978, 6: 461-464. 10.1214/aos/1176344136.View ArticleGoogle Scholar
- Link WA, Barker RJ: Model weights and the foundations of multimodel inference. Ecology. 2006, 87: 2626-2635. 10.1890/0012-9658(2006)87[2626:MWATFO]2.0.CO;2.View ArticlePubMedGoogle Scholar
- Krahn MM, Ford MJ, Perrin WF, Wade PR, Angliss RP, Hanson MB, Taylor BL, Ylitalo GM, Dahlheim ME, Stein JE, Waples RS: Status review of Southern Resident killer whales (Orcinus orca) under the Endangered Species Act. 2004, US Dept Commer, NMFS-NWFSC-62, 72-Google Scholar
- Weladji RB, Gaillard JM, Yoccoz NG, Holand O, Mysterud A, Loison A, Nieminen M, Stenseth NC: Good reindeer mothers live longer and become better in raising offspring. Proceedings of the Royal Society B-Biological Sciences. 2006, 273: 1239-1244. 10.1098/rspb.2005.3393.PubMed CentralView ArticleGoogle Scholar
- McGraw JB, Caswell H: Estimation of individual fitness from life-history data. American Naturalist. 1996, 147: 47-64. 10.1086/285839.View ArticleGoogle Scholar
- Clutton-Brock T, Albon SD, Guinness FE: Reproductive success in male and female red deer. Reproductive success. Edited by: Clutton-Brock TH. 1988, University of Chicago Press, 325-343.Google Scholar
- Brommer JE, Gustafsson L, Pietiainen H, Merila J: Single-generation estimates of individual fitness as proxies for long-term genetic contribution. American Naturalist. 2004, 163: 505-517. 10.1086/382547.View ArticlePubMedGoogle Scholar
- Tuljapurkar SD, Puleston CO, Gurven MD: Why Men Matter: Mating Patterns Drive Evolution of Human Lifespan. PLoS ONE. 2007, 2: e785-10.1371/journal.pone.0000785.PubMed CentralView ArticlePubMedGoogle Scholar
- Pavard S, Metcalf CJE, Heyer E: Senescence of Reproduction may Explain Adaptive Menopause in Humans: A Test of the "Mother" Hypothesis. American Journal of Physical Anthropology. 2008, 136: 194-203. 10.1002/ajpa.20794.View ArticlePubMedGoogle Scholar
- Sear R, Mace R: Who keeps children alive? A review of the effects of kin on child survival. Evolution and Human Behavior. 2008, 29: 1-18. 10.1016/j.evolhumbehav.2007.10.001.View ArticleGoogle Scholar
- Shanley DP, Sear R, Mace R, Kirkwood TBL: Testing evolutionary theories of menopause. Proceedings of the Royal Society B-Biological Sciences. 2007, 274: 2943-2949. 10.1098/rspb.2007.1028.PubMed CentralView ArticleGoogle Scholar
- Lusseau D: Why Are Male Social Relationships Complex in the Doubtful Sound Bottlenose Dolphin Population?. PLoS ONE. 2007, 2: e348-10.1371/journal.pone.0000348.PubMed CentralView ArticlePubMedGoogle Scholar
This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.