Filial Cannibalism in the Biparental Fish Cichlasoma nigrofasciatum (Pisces: Cichlidae) in Response to Early Brood Reductions

Filial cannibalism (eating one's own offspring) may enhance a parent's lifetime reproductive success if the costs associated with this behaviour are outweighed by its benefits. An organism might limit its parental care to relatively high quality offspring and eat the others. Or, an organism capable of repeated breeding in the same season might eat the survivors of a brood that was reduced by predators, and breed again. In this study, we manipulated brood size of convict cichlids by removing 0 % (control), 33 % (ER 33) or 66 % (ER 66) of the eggs spawned. The results show that smaller broods are more likely to be cannibalized by their parent(s) than are larger broods. Furthermore, pairs with reduced broods were preparing to respawn; female gonad weights were significantly higher in the brood-reduction groups than in the control group. In a second experiment, we show that the behaviour of the parents differed significantly between experimental groups; the ER 66 group performed less parental care than the control group. Moreover, females invested more parental effort than males. The results suggest that filial cannibalism may be a tactic used by parental convict cichlids to enhance their lifetime reproductive success.     

Offspring of older parents are smaller—but no less bilaterally symmetrical—than offspring of younger parents in the aquatic plant Lemna turionifera

Offspring quality decreases with parental age in many taxa, with offspring of older parents exhibiting reduced life span, reproductive capacity, and fitness, compared to offspring of younger parents. These “parental age effects,” whose consequences arise in the next generation, can be considered as manifestations of parental senescence, in addition to the more familiar age‐related declines in parent‐generation survival and reproduction. Parental age effects are important because they may have feedback effects on the evolution of demographic trajectories and longevity. In addition to altering the timing of offspring life‐history milestones, parental age effects can also have a negative impact on offspring size, with offspring of older parents being smaller than offspring of younger parents. Here, we consider the effects of advancing parental age on a different aspect of offspring morphology, body symmetry. In this study, we followed all 403 offspring of 30 parents of a bilaterally symmetrical, clonally reproducing aquatic plant species, Lemna turionifera, to test the hypothesis that successive offspring become less symmetrical as their parent ages, using the “Continuous Symmetry Measure” as an index. Although successive offspring of aging parents older than one week became smaller and smaller, we found scant evidence for any reduction in bilateral symmetry.     

Evidence for male alternative reproductive tactics in convict cichlids (<Emphasis Type="Italic">Amatitlania siquia</Emphasis>) in Lake Xiloá, Nicaragua

We present evidence suggesting that some male convict cichlids (Amatitlania siquia) in Lake Xiloá, Nicaragua engage in alternative reproductive tactics (ARTs). These putative ART males were smaller than typical parental males, displayed coloration similar to breeding females, and possessed enlarged gonads. Gonadosomatic indices in these males were 16-fold higher than parental males and three-fold higher than females. This phenotype is consistent with the ‘sneaker’ or ‘satellite’ phenotype reported in other species. A survey of 282 fish in 2014 found three males (1% of all fish, 2% of males) with these characteristics. This finding is significant because convict cichlids are frequently studied in laboratory and field in the context of monogamy and biparental care.     

Sex Differences in Retrieval Behavior by the Biparental Convict Cichlid

Biparental species occasionally demonstrate a division of roles in which parents perform sex-typical tasks, with females offering direct care and spending the majority of their time with the offspring while males are more indirect in their care, providing the majority of defense against potential brood predators. To examine the flexibility in the sex-typical roles shown by convict cichlids ( Amatitlania nigrofasciata ), we displaced non-swimming young at three different distances from the nest and then analyzed the retrieval behaviors of each parent. Retrieval of altricial young is a behavior commonly used to measure parental care in mammalian studies, but has rarely been used in other taxa. We found sex differences in retrieval behavior: on average, females retrieved young close to the nest and males retrieved young far from the nest. This difference in parental contribution suggests a division of labor with sex-specific roles. Sex differences may be due to proximity to young and/or apparent risk of offspring predation. Additionally, we found that latency to first retrieval and total time spent retrieving young remained consistent across the various displacement distances, suggesting that retrieval is an essential parental behavior. Additionally, we include observations of wriggler retrieval by parents in a natural population of Costa Rican convict cichlids.     

Contrasting Parental Tasks Influence Parental Roles for Paired and Single Biparental Cichlid Fish

Biparental care of young occurs when both parents provide some sort of care for offspring and can include a wide variety of behaviors, yet often studies focus on single aspects of parental care when trying to determine how each parent contributes. Here, we presented the biparental convict cichlid fish (Amatitlania nigrofasciata) with two conflicting parental behaviors: retrieval of non‐swimming offspring that have been displaced from the nest and defense against a conspecific intruder, a potential brood predator. We examined single males, single females, and pairs of parents to determine how males and females each contributed to overall parental care. Traditionally in this species, parents exhibit a division of labor (in which each parent contributes to all parental activities), but also exhibit a division of roles (in which males tend to favor the role of defense and females tend to favor more direct care, spending more time with offspring). We hypothesized that single parents would compensate for their absent mate, but that males and females would still favor preferred roles. Additionally, we hypothesized that there would be an asymmetrical expansion of roles, with females being more flexible. Our results show that the preferred roles of both parents were evident even when parents were without their mates and that males and females differed in their compensatory levels, at least when compared to the behaviors of the intact pair. Contrary to our prediction, females seem unable to fully compensate for the defensive behaviors usually exhibited by males, while males shifted completely to retrieve displaced offspring.     

Sex-dependent risk taking in the collared flycatcher, Ficedula albicollis, when exposed to a predator at the nestling stage

An increased mortality rate is a cost of parental care, and can be high during the provisioning phase of altricial nestlings. When a parent stops feeding the nestlings temporarily after seeing a predator, it can reduce its own predation risk, but the suspension of parental care may also reduce its offspring's chances of surviving. We modelled this situation by exposing a stuffed sparrowhawk near collared flycatcher nests and removing it when both parents had seen it. We measured the time (return time) between the removal and when each parent entered the nestbox. The parents' risk taking and the return time are assumed to be inversely related. We studied which brood variables the parents take into account when deciding how much risk they are willing to take during the provisioning period. Males took more risk for older and better-quality nestlings and earlier broods. The females' behaviour was opposite to that of the males: they took significantly less risk for older and better-quality offspring and visited the nestbox later for earlier broods. The males' behaviour supported the reproductive value hypothesis, that risk taking is related to brood value and survival chances, whereas the females' behaviour supported the harm to offspring hypothesis, that risk taking is related to the broods' vulnerability. Copyright 2000 The Association for the Study of Animal Behaviour.     

Seasonal Variation in Parental Care Drives Sex-Specific Foraging by a Monomorphic Seabird

Evidence of sex-specific foraging in monomorphic seabirds is increasing though the underlying mechanisms remain poorly understood. We investigate differential parental care as a mechanism for sex-specific foraging in monomorphic Common Murres (Uria aalge), where the male parent alone provisions the chick after colony departure. Using a combination of geolocation-immersion loggers and stable isotopes, we assess two hypotheses: the reproductive role specialization hypothesis and the energetic constraint hypothesis. We compare the foraging behavior of females (n = 15) and males (n = 9) during bi-parental at the colony, post-fledging male-only parental care and winter when parental care is absent. As predicted by the reproductive role specialization hypothesis, we found evidence of sex-specific foraging during post-fledging only, the stage with the greatest divergence in parental care roles. Single-parenting males spent almost twice as much time diving per day and foraged at lower quality prey patches relative to independent females. This implies a potential energetic constraint for males during the estimated 62.8 ± 8.9 days of offspring dependence at sea. Contrary to the predictions of the energetic constraint hypothesis, we found no evidence of sex-specific foraging during biparental care, suggesting that male parents did not forage for their own benefit before colony departure in anticipation of post-fledging energy constraints. We hypothesize that unpredictable prey conditions at Newfoundland colonies in recent years may limit male parental ability to allocate additional time and energy to self-feeding during biparental care, without compromising chick survival. Our findings support differential parental care as a mechanism for sex-specific foraging in monomorphic murres, and highlight the need to consider ecological context in the interpretation of sex-specific foraging behavior.     

Parent age differentially influences offspring size over the course of development in Laysan albatross

Offspring growth and survival are predicted to be higher for older parents, due to a variety of mechanisms, such as increased breeding experience or greater investment favored by low residual reproductive value. Yet the extent to which parent age affects offspring viability is likely to vary between different aspects of growth and survival, perhaps being most pronounced at the most stressful stages of reproduction. We studied the link between parent age and nestling growth and survival in the Laysan albatross, a long-lived seabird with a mean first breeding age of 8 years. Offspring of older parents were more likely to survive to fledging. Among those that did fledge, nestlings of older parents grew more rapidly. However, parent age did not influence the eventual asymptotic size that nestlings reached before fledging: fast-growing nestlings of older parents reached 90% of asymptotic size roughly 1 week sooner, but slow-growing nestlings of younger parents eventually caught up in size before fledging. Older parents bred c . 2 days earlier than younger parents, but hatch date did not explain observed variation in offspring success. The extent to which parent age accounted for variation in size of individual nestlings was not constant but peaked near the midpoint of development. This could reflect a time period when demands on parents reveal age-based differences in parental quality. Overall, growth and survival of offspring increased with parent age in this species, even though the late age of first breeding potentially provides a 7-year period for birds to hone their foraging skills or for selection to eliminate low-quality individuals.     

The risks of parenthood. I. General theory and applications

Summary We use contemporary life history theory to analyze parental decisions concerned with the defense of offspring, and with the provisioning of offspring in the presence of risk. In achieving the optimal level of parental investment, the parent faces a tradeoff between present and future reproductive success. Our models, which are based on stochastic dynamic programming, lead to predictions of the following kind: (i) offspring will be defended more vigorously as they grow older; (ii) long-lived species will accept fewer risks in caring for offspring than short-lived species; (iii) parents living in permanently riskier environments will defend their offspring more vigorously than parents in less risky environments; (iv) however, temporary increases in risk will result in temporarily less vigorous defense and provisioning of offspring. The models also show that parents and their offspring have different conceptions of the optimal level of parental investment. The flexibility of our modeling approach as a method of analyzing facultative behavior is also emphasized. Finally, we apply the methods of this paper to analyze fledging behavior of Atlantic puffins.     

Common loon parents defend chicks according to both value and vulnerability

In many territorial breeders, conspecifics that intrude during the chick‐rearing period pose a threat to survival of young. Defense of young from intruders is costly to parents, so it is likely that intense selective pressure has shaped chick defense so as to maximize parental fitness. We simulated territorial intrusion by exposing adult common loons Gavia immer and their chicks to a decoy and used mixed models to investigate responses. We tested two hypotheses: 1) the value hypothesis, which holds that parents should defend large broods of offspring more strongly because of the greater potential fitness benefits they offer, and 2) the vulnerability hypothesis, which predicts vigorous defense of young offspring, whose small size and limited mobility render them vulnerable to sudden attacks from intruders that approach under water. Under natural conditions, parents spent over 80% of their time within 20 m of chicks younger than two weeks (‘young chicks’) but 66% or less of their time close to chicks four weeks or older (‘old chicks’). Parents of young chicks associated less with the decoy but yodelled and penguin danced more during decoy trials than did parents of old chicks, supporting the conclusion that the parents protected young chicks not by engaging intruders directly but by remaining close to chicks and using vocalization and display to keep intruders at a distance. While these findings lent clear support to the vulnerability hypothesis, the value hypothesis too was supported, as males with two‐chick broods were almost three times more likely to yodel than males with singleton chicks. Age of parents was not associated with any aspect of chick defense, but the paucity of known‐aged parents in the oldest age classes makes future investigation of age effects warranted.     

Inclusive fitness effects can select for cancer suppression into old age

Natural selection can favour health at youth or middle age (high reproductive value) over health at old age (low reproductive value). This means, all else being equal, selection for cancer suppression should dramatically drop after reproductive age. However, in species with significant parental investment, the capacity to enhance inclusive fitness may increase the reproductive value of older individuals or even those past reproductive age. Variation in parental investment levels could therefore contribute to variation in cancer susceptibility across species. In this article, we describe a simple model and framework for the evolution of cancer suppression with varying levels of parental investment and use this model to make testable predictions about variation in cancer suppression across species. This model can be extended to show that selection for cancer suppression is stronger in species with cooperative breeding systems and intergenerational transfers. We consider three cases that can select for cancer suppression into old age: (i) extended parental care that increases the survivorship of their offspring, (ii) grandparents contributing to higher fecundity of their children and (iii) cooperative breeding where helpers forgo reproduction or even survivorship to assist parents in having higher fecundity.     

Sexual selection determines parental care patterns in cichlid fishes

Despite a massive research effort, our understanding of why, in most vertebrates, males compete for mates and females care for offspring remains incomplete. Two alternative hypotheses have been proposed to explain the direction of causality between parental care and sexual selection. Traditionally, sexual selection has been explained as a consequence of relative parental investment, where the sex investing less will compete for the sex investing more. However, a more recent model suggests that parental care patterns result from sexual selection acting on one sex favoring mating competition and lower parental investment. Using species-level comparative analyses on Tanganyikan cichlid fishes we tested these alternative hypotheses employing a proxy of sexual selection based on mating system, sexual dichromatism, and dimorphism data. First, while controlling for female reproductive investment, we found that species with intense sexual selection were associated with female-only care whereas species with moderate sexual selection were associated with biparental care. Second, using contingency analyses, we found that, contrary to the traditional view, evolutionary changes in parental care type are dependent on the intensity of sexual selection. Hence, our results support the hypothesis that sexual selection determines parental care patterns in Tanganyikan cichlid fishes.     

Control of parental investment changes plastically over time with residual reproductive value

Evolutionary conflict between parents and offspring over parental resource investment is a significant selective force on the traits of both parents and offspring. Empirical studies have shown that for some species, the amount of parental investment is controlled by the parents, whereas in other species, it is controlled by the offspring. The main difference between these two strategies is the residual reproductive value of the parents or opportunities for future reproduction. Therefore, this could explain the patterns of control of parental investment at the species level. However, the residual reproductive value of the parents will change during their lifetime; therefore, parental influence on the amount of investment can be expected to change plastically. Here, we investigated control of parental investment when parents were young and had a high residual reproductive value, compared to when they were old and had a low residual reproductive value using a cross‐fostering experiment in the burying beetle Nicrophorus quadripunctatus. We found that parents exert greater control over parental investment when they are young, but parental control is weakened as the parents age. Our results demonstrate that control of parental investment is not fixed, but changes plastically during the parent's lifetime.     

The pay‐offs of maternal care increase as offspring develop,favouring extended provisioning in an egg‐feeding frog

Offspring quantity and quality are components of parental fitness that cannot be maximized simultaneously. When the benefits of investing in offspring quality decline, parents are expected to shift investment towards offspring quantity (other reproductive opportunities). Even when mothers retain complete control of resource allocation, offspring control whether to allocate investment to growth or development towards independence, and this shared control may generate parent–offspring conflict over the duration of care. We examined these predictions by, in a captive colony, experimentally removing tadpoles of the strawberry poison frog (Oophaga pumilio) from the mothers that provision them with trophic eggs throughout development. Tadpoles removed from their mothers were no less likely to survive to nutritional independence (i.e. through metamorphosis) than were those that remained with their mothers, but these offspring were smaller at metamorphosis and were less likely to survive to reach adult size, even though they were fed ad libitum. Tadpoles that remained with their mothers developed more slowly than those not receiving care, a pattern that might suggest that offspring extracted more care than was in mothers’ best interests. However, the fitness returns of providing care increased with offspring development, suggesting that mothers would be best off continuing care until tadpoles initiated metamorphosis. Although the benefits of parental investment in offspring quality are often thought to asymptote at high levels, driving parent–offspring conflict over weaning, this assumption may not hold over natural ranges of investment, with selection on both parents and offspring favouring extended durations of parental care.     

Morphological and genetic predictors of parental care in the North American barn swallow Hirundo rustica erythrogaster

Sexually dimorphic traits often signal the fitness benefits an individual can provide to potential mates. In species with altricial young, these signals may also predict the level of parental care an individual is expected to provide to shared offspring. In this study, we tested three hypotheses that traditionally relate sexually dimorphic traits to parental care in two populations of North American barn swallows Hirundo rustica erythrogaster. The good parent hypothesis predicts a positive relationship between an individual's ornamentation and his or her care whereas the differential allocation (more care given by individuals when paired to high quality mates) and reproductive compensation (more care given by individuals when paired to low quality mates) hypotheses predict that an individual's level of parental investment is relative to the quality of their mate. Male and female North American barn swallows have colorful ventral feathers and elongated tail streamers, but there is evidence that ventral color, not tail streamer length, predicts measures of seasonal reproductive success. Accounting for the positive correlation between within‐pair feeding rates and other potentially confounding variables in all of our models, we found no support for the good parent hypothesis because in both males and females, traits shown to be under sexual selection did not predict feeding rates in either sex. However, our data reveal that male coloration, and not streamer length, predicted a female's provisioning rate to shared offspring (females fed more when paired with darker individuals) in two separate populations, supporting the differential allocation, but not the reproductive compensation hypothesis. Because genetic traits have also been shown to affect parental investment, we evaluated this variable as well and found that a male's paternity did not have significant effects on either male or female feeding rates. Overall, our results suggest that females do not pair with darker males in order to gain direct benefits in terms of his expected levels of parental care to shared offspring, but do themselves invest greater levels of care when paired to darker males. Further, our results are consistent with previous studies which suggest that ventral feather color, not streamer length, is a target of sexual selection in North American populations of barn swallow because females invested more in their offspring when paired to darker mates.     

Foster rather than biological parental telomere length predicts offspring survival and telomere length in king penguins

Because telomere length and dynamics relate to individual growth, reproductive investment and survival, telomeres have emerged as possible markers of individual quality. Here, we tested the hypothesis that, in species with parental care, parental telomere length can be a marker of parental quality that predicts offspring phenotype and survival. In king penguins (Aptenodytes patagonicus), we experimentally swapped the single egg of 66 breeding pairs just after egg laying to disentangle the contribution of prelaying parental quality (e.g., genetics, investment in the egg) and/or postlaying parental quality (e.g., incubation, postnatal feeding rate) on offspring growth, telomere length and survival. Parental quality was estimated through the joint effects of biological and foster parent telomere length on offspring traits, both soon after hatching (day 10) and at the end of the prewinter growth period (day 105). We expected that offspring traits would be mostly related to the telomere lengths (i.e., quality) of biological parents at day 10 and to the telomere lengths of foster parents at day 105. Results show that chick survival up to 10 days was negatively related to biological fathers’ telomere length, whereas survival up to 105 days was positively related to foster fathers’ telomere lengths. Chick growth was not related to either biological or foster parents’ telomere length. Chick telomere length was positively related to foster mothers’ telomere length at both 10 and 105 days. Overall, our study shows that, in a species with biparental care, parents’ telomere length is foremost a proxy of postlaying parental care quality, supporting the “telomere – parental quality hypothesis.”     

Terminal investment and senescence in rhesus macaques (Macaca mulatta) on Cayo Santiago

Long-lived iteroparous species often show aging-related changes in reproduction that may be explained by 2 non-mutually exclusive hypotheses. The terminal investment hypothesis predicts increased female reproductive effort toward the end of the life span, as individuals have little to gain by reserving effort for the future. The senescence hypothesis predicts decreased female reproductive output toward the end of the life span due to an age-related decline in body condition. Nonhuman primates are ideal organisms for testing these hypotheses, as they are long lived and produce altricial offspring heavily dependent on maternal investment. In this study, we integrated 50 years of continuous demographic records for the Cayo Santiago rhesus macaque (Macaca mulatta) population with new morphometric and behavioral data to test the senescence and terminal investment hypotheses. We examined relationships between maternal age and activity, mother and infant body condition, interbirth intervals, measures of behavioral investment in offspring, and offspring survival and fitness to test for age-associated declines in reproduction that would indicate senescence, and for age-associated increases in maternal effort that would indicate terminal investment. Compared with younger mothers, older mothers had lower body mass indices and were less active, had longer interbirth intervals, and spent more time in contact with infants, but had infants of lower masses and survival rates. Taken together, our results provide strong evidence for the occurrence of reproductive senescence in free-ranging female rhesus macaques but are also consistent with some of the predictions of the terminal investment hypothesis.     

Female blue tits adjust parental effort to manipulated male UV attractiveness

The differential allocation hypothesis predicts that parents should adjust their current investment in relation to perceived mate attractiveness if this affects offspring fitness. It should be selectively advantageous to risk more of their future reproductive success by investing heavily in current offspring of high reproductive value but to decrease investment if offspring value is low. If the benefits of mate attractiveness are limited to a particular offspring sex we would instead expect relative investment in male versus female offspring to vary with mate attractiveness, referred to as 'differential sex allocation'. We present strong evidence for differential allocation of parental feeding effort in the wild and show an immediate effect on a component of offspring fitness. By experimentally reducing male UV crown coloration, a trait known to indicate attractiveness and viability in wild-breeding blue tits (Parus caeruleus), we show that females, but not males, reduce parental feeding rates and that this reduces the skeletal growth of offspring. However, differential sex allocation does not occur. We conclude that blue tit females use male UV coloration as an indicator of expected offspring fitness and adjust their investment accordingly.     

Greater opportunities for sexual selection in male than in female obligate brood parasitic birds

Females are expected to have evolved to be more discriminatory in mate choice than males as a result of greater reproductive investment into larger gametes (eggs vs. sperm). In turn, males are predicted to be more promiscuous than females, showing both a larger variance in the number of mates and a greater increase in reproductive success with more mates, yielding more intense sexual selection on males vs. females (Bateman's Paradigm). However, sex differences in costly parental care strategies can either reinforce or counteract the initial asymmetry in reproductive investment, which may be one cause for some studies failing to conform with predictions of Bateman's Paradigm. For example, in many bird species with small female‐biased initial investment but extensive biparental care, both sexes should be subject to similar strengths of sexual selection because males and females are similarly restricted in their ability to pursue additional mates. Unlike 99% of avian species, however, obligate brood parasitic birds lack any parental care in either sex, predicting a conformation to Bateman's Paradigm. Here we use microsatellite genotyping to demonstrate that in brood parasitic brown‐headed cowbirds (Molothrus ater), per capita annual reproductive success increases with the number of mates in males, but not in females. Furthermore, also as predicted, the variance of the number of mates and offspring is greater in males than in females. Thus, contrary to previous findings in this species, our results conform to predictions of the Bateman's Paradigm for taxa without parental care.     

How does a parent respond when its mate emphasizes the wrong role? A test using a monogamous fish

The convict cichlid fish, Archocentrus nigrofasciatus, is biparental: the male spends the majority of his time defending the territory and the female spends much of her time close to the offspring. Under natural conditions, this separation into sex-typical roles is somewhat blurred as males do spend some time with the offspring and females do attack intruders. Here we tested whether an individual selects a parental role based on the location (i.e. parental role) of its mate. For example, do females emphasize offspring care because the male is away from the offspring? Will males be more likely to care for the offspring when the female is away from the offspring? We manipulated the location of one parent by placing it in a transparent plastic box, either near the offspring or at the far end of the tank near a clear plastic compartment that held a conspecific male intruder. We tested both male and female parent under the following four conditions: boxed mate near offspring with no intruder present, boxed mate near offspring with intruder present, boxed mate near intruder compartment with no intruder present, and boxed mate near intruder compartment with intruder present. We found that both parents spent more time with the offspring and less time attacking the intruder when the mate was positioned near the offspring and more time away from the offspring and more time attacking the intruder when the mate was near the intruder. Males were more affected by the location of their mates than were females and we concluded that males were attracted both to their mates' location and their offspring while females were mostly attracted to their offspring. Overall, the location of the mate had little effect on the types of aggressive activities used against the intruder. We did find that males increased their aggression towards boxed females when they were positioned far from the offspring, whereas the aggressive behaviour of females towards boxed males when they were positioned near the offspring was ambiguous. We suggest that males in particular enforce the separation of sex-specific parental roles via this aggression.