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.     

A large population parental care game: Polymorphisms and feedback between patterns of care and the operational sex ratio

This article presents a game theoretic model of parental care which models the feedback between patterns of care and the operational sex ratio. It is assumed here that males can be in one of two states: searching for a mate or breeding (including caring for their offspring). Females can be in one of three states: receptive (searching), non-receptive or breeding. However, these sets of states can be adapted to the physiology of a particular species. The length of time that an individual remains in the breeding state depends on the level of care an individual gives. When in the searching state, individuals find partners at a rate dependent on the proportion of members of the opposite sex searching. These rates are defined to satisfy the Fisher condition that the total number of offspring of males equals the total number of offspring of females. The operational sex ratio is not defined exogenously, but can be derived from the adult sex ratio and the pattern of parental care. Pure strategy profiles and so-called single sex stable polymorphisms, in which behaviour is varied within one sex, are derived analytically. The difference between mixed evolutionarily stable strategies and stable polymorphisms within this framework is highlighted. The effects of various physiological and demographic parameters on patterns of care are considered.     

The evolution of parental care

Our understanding of parental care behavior can be significantly advanced through the application of Williams's Principle, which states that reproduction has not only a benefit but also a cost to lifetime fitness. My laboratory has formalized Williams's Principle into the relative value theorem and found that its application to fishes, the taxa with the most diverse patterns of parental care, can help to explain which sex provides care and how much. In fishes, it is often the male that provides parental care, not because the male obtains greater benefits from this care, but probably because he pays fewer costs. Fish dynamically adjust their investment into parental care according to the number of offspring in their brood, past investment, genetic relatedness, and alternative mating opportunities, all of which affect the value of current offspring relative to potential future offspring. These results may also help us understand the joy and the challenges of parental care in humans.     

The evolution of avian parental care

A stage model traces key behavioural tactics and life-history traits that are involved in the transition from promiscuity with no parental care, the mating system that typifies reptiles, to that typical of most birds, social monogamy with biparental care. In stage I, females assumed increasing parental investment in precocial young, female choice of mates increased, female-biased mating dispersal evolved and population sex ratios became male biased. In stage II, consortships between mating partners allowed males to attract rare social mates, provided a mechanism for paternity assessment and increased female ability to assess mate quality. In stage III, relative female scarcity enabled females to demand parental investment contributions from males having some paternity certainty. This innovation was facilitated by the nature of avian parental care; i.e. most care-giving activities can be adopted in small units. Moreover, the initial cost of care giving to males was small compared with its benefit to females. Males, however, tended to decline to assume non-partitionable, risky, or relatively costly parental activities. In stage IV, altriciality coevolved with increasing biparental care, resulting in social monogamy. Approaches for testing behavioural hypotheses are suggested.     

The post‐fledging period in a tropical bird: patterns of parental care and survival

How environmental conditions affect the timing and extent of parental care is a fundamental question in comparative studies of life histories. The post‐fledging period is deemed critical for offspring fitness, yet few studies have examined this period, particularly in tropical birds. Tropical birds are predicted to have extended parental care during the post‐fledging period and this period may be key to understanding geographic variation in avian reproductive strategies. We studied a neotropical passerine, the western slaty‐antshrike Thamnophilus atrinucha, and predicted greater care and higher survival during the post‐fledging period compared to earlier stages. Furthermore, we predicted that duration of post‐fledging parental care and survival would be at the upper end of the distribution for Northern Hemisphere passerines. Correspondingly, we observed that provisioning continued for 6–12 weeks after fledging. In addition, provisioning rate was greater after fledging and offspring survival from fledging to independence was 75%, greater than all estimates from north‐temperate passerines. Intervals between nesting attempts were longer when the first brood produced successful fledglings compared to nests where offspring died either in the nest or upon fledging. Parents delayed initiating second nests after the first successful brood until fledglings were near independence. Our results indicate that parents provide greater care after fledging and this extended care likely increased offspring survival. Moreover, our findings of extended post‐fledging parental care and higher post‐fledging survival compared to Northern Hemisphere species have implications for understanding latitudinal variation in reproductive effort and parental investment strategies.     

鱼类亲代抚育行为的研究进展

亲代抚育行为（parental care behavior）是指动物对其后代或其亲缘后代提供保护和养育的所有活动,属于本能行为的一种,广泛存在于动物界之中。鱼类在其为数不多的科中充分发展了几乎所有类型的亲代抚育行为,因而成为研究该行为的最佳物种之一。随着威廉斯原理（Williams’s Principle）的提出和应用,人们对鱼类亲代抚育行为的探索逐步由定性向定量发展,普遍认同了在鱼类进化中,雄性抚育模式得以占据支配地位的缘由并非是因为雄性在抚育活动中获得了较多的利益,而是由于在获取相同利益时雄性损失的未来投资成本较雌性低的观点。近年来的研究证实,在亲代抚育过程中存在着某种动态调整机制,其中四个比较关键的影响因素分别为：亲本所抚育的子代数量、亲本先前的投资、亲本与被抚育子代间的遗传关联度和亲本未来的交配机会。     

The phylogeny of parental care in fishes

This paper tests the hypothesis that in the evolution of parental care, taxa of bony fish should only exhibit certain transitional states (where a transition is defined by the occurrence of at least two types of parental care within a genus or family). These are those between no parental care and male care, male care and biparental care, biparental care and female care, and female care and no parental care. A review of the teleost literature reveals 21 transitions. All of these agree with the hypothesized transitions and, in some cases, the direction of evolution is inferred by simple pedigree analysis.     

A dynamic game-theoretic model of parental care

We present a model in which members of a mated pair decide whether to care for their offspring or desert them. There is a breeding season of finite length during which it is possible to produce and raise several batches of offspring. On deserting its offspring, an individual can search for a new mate. The probability of finding a mate depends on the number of individuals of each sex that are searching, which in turn depends upon the previous care and desertion decisions of all population members. We find the evolutionarily stable pattern of care over the breeding season. The feedback between behaviour and mating opportunity can result in a pattern of stable oscillations between different forms of care over the breeding season. Oscillations can also arise because the best thing for an individual to do at a particular time in the season depends on future behaviour of all population members. In the baseline model, a pair splits up after a breeding attempt, even if they both care for the offspring. In a version of the model in which a pair stays together if they both care, the feedback between behaviour and mating opportunity can lead to more than one evolutionarily stable form of care.     

Innovative parental care in a myrmecophageous mammal

Male bat-eared foxes, Otocyon megalotis, are known to contribute extensively to parental care. Yet, the exact roles that males and females play in raising offspring remain relatively unexplored. Here, we describe interactions between adult foxes and their presumed offspring based on a pilot study on three family groups of a wild population in South Africa. We report the first recorded instance of dung provisioning observed in canids. A male bat-eared fox provided dung to his offspring during a foraging trip, presumably to give them access to the ensconced insects. Further, this male provisioned the young foxes with large, live insects. Similar to other researchers, we never observed provisioning by females, but the females in this population did interact socially with their young in addition to suckling. We emphasize the importance of anecdotal reports of novel behavioural responses in wild canids, as an accumulation of such evidence may reveal patterns of innovative behaviour presently unrecognized in this family.     

The evolution of parental care in freshwater leeches

Summary The life-history strategies of a selection of the most common European freshwater leeches (Euhirudinea) are described. On the basis of this information and results from the literature, the probable phylogenetic development of parental care in the Euhirudinea is reconstructed. The jawless worm leeches (Erpobdellidae) secrete a protective cocoon, cement it to the substrate and sometimes ventilate it before they leave the egg capsules. This behaviour represents the most ancient state in leech evolution. Members of the jawed Hirudinidae deposit desiccation-resistant cocoons on land. All known Glossiphoniidae (leeches equipped with a proboscis) have evolved the habit of brooding the eggs and young. These unique parental care patterns within one family of extant freshwater leeches can be arranged schematically in a series of increasing complexity which may reflect the evolution of brooding behaviour. Glossiphoniid leeches of the genus Helobdella, which have a world-wide distribution, display the most highly developed parental care system: they not only protect but also feed the young they carry. This results in the young being much larger when they leave the parent and, presumably, in higher subsequent survival. Isolated cocoons of all aquatic leeches are rapidly destroyed by predators, primarily water snails. In erpobdellids (but not glossiphoniids, which protect the cocoons) a large portion of the cocoons are lost due to predatory attacks. We conclude that the major selective pressure driving the evolution of parental care in leeches may have been predation on eggs and juvenile stages. Dedicated to Professor Dr. G. Osche on the occasion of his 75th birthday     

Paternity and the evolution of male parental care

It is generally believed that level of paternity (the proportion of zygotes in a brood that were fertilized by the male providing parental care) has an important role in the evolution of parental care. We have used population genetics models to investigate this role. The models indicate that only in mating systems where a parental male “sacrifices” promiscous matings can paternity influence the evolution of male parental care. This is because level of paternity can reflect the number of opportunities for these promiscuous fertilizations. For example, high paternity can mean few opportunities and therefore a low cost for paternal care.Certain behaviors may preadapt a species for the evolution of male parental care because they decrease the costs of providing care. For example, in fish species where male care has evolved from spawning territories, the very establishment of territories may have precluded males from gaining promiscuous matings, thereby eliminating the promiscuity costs and facilitating the evolution of care. Without a promiscuity cost, level of paternity will not have influenced the evolution of male care in fishes.Because paternity has limited influence in the evolution of male care, differences in reliability of parentage between males and females are unlikely to explain the prevalence of female care. Our analysis suggests that paternity differences between species cannot serve as a general explanation for the observed patterns of parental care behavior.     

The evolution of parental care in stochastic environments

Parental care is of fundamental importance to understanding reproductive strategies and allocation decisions. Here, we explore how parental care strategies evolve in variable environments. Using a set of life-history trait trade-offs, we explore the relative costs and benefits of parental care in stochastic environments. Specifically, we consider the cases in which environmental variability results in varying adult death rates, egg death rates, reproductive rate and carrying capacity. Using a measure of fitness appropriate for stochastic environments, we find that parental care has the potential to evolve over a wide range of life-history characteristics when the environment is variable. A variable environment that affects adult or egg death rates can either increase or decrease the fitness of care relative to that in a constant environment, depending on the specific costs of care. Variability that affects carrying capacity or adult reproductive rate has negligible effects on the fitness associated with care. Increasing parental care across different life-history stages can increase fitness gains in variable environments. Costly investment in care is expected to affect the overall fitness benefits, the fitness optimum and rate of evolution of parental care. In general, we find that environmental variability, the life-history traits affected by such variability and the specific costs of care interact to determine whether care will be favoured in a variable environment and what levels of care will be selected.     

A new mode of parental care in cockroaches

Summary A new form of maternal provisioning of newly hatched nymphs is described in the ovoviviparous cockroach Gromphadorhina portentosa. Shortly after expelling the hatching egg case, the female exudes from her abdominal tip a whitish, translucent material on which neonates actively feed. Integumentary gland cells lining the brood sac are the most likely source of the secretion. This form of maternal provisioning may not be restricted to the Madagascar hissing cockroach; a glandular brood sac similar to that of G. portentosa is found in at least three additional ovoviviparous cockroaches.Received 22 January 2003; revised 4 March 2003; accepted 19 March 2003.     

Evolution of parental care driven by mutual reinforcement of parental food provisioning and sibling competition

In mammals, altricial birds and some invertebrates, parents care for their offspring by providing them with food and protection until independence. Although parental food provisioning is often essential for offspring survival and growth, very little is known about the conditions favouring the evolutionary innovation of this key component of care. Here, we develop a mathematical model for the evolution of parental food provisioning. We find that this evolutionary innovation is favoured when the efficiency of parental food provisioning is high relative to the efficiency of offspring self-feeding and/or parental guarding. We also explore the coevolution between food provisioning and other components of parental care, as well as offspring behaviour. We find that the evolution of food provisioning prompts evolutionary changes in other components of care by allowing parents to choose safer nest sites, and that it promotes the evolution of sibling competition, which in turn further drives the evolution of parental food provisioning. This mutual reinforcement of parental care and sibling competition suggests that evolution of parental food provisioning should show a unidirectional trend from no parental food provisioning to full parental food provisioning.     

Fertilization mode, sperm characteristics, mate choice and parental care patterns in Artedius spp. (Cottidae)

The reproductive biology of three species in the genus Artedius ( A. harringtoni, A. lateralis and A. fenestralis ) was studied, including parental behaviour, mate choice, fertilization mode, gamete morphology and behaviour, and gonad morphology to help understand the coevolution of reproductive characteristics with potentially different modes of fertilization. In all three species, males guard multiple clutches at oviposition sites. In laboratory mate‐choice experiments, males appearred to prefer to defend sites containing eggs and were better able to attract mates at these sites. There was evidence that internal gomete association, although more pronounced in A. harringtoni , existed in all three species. Sperm behaviour and morphology and histological analysis of gonads suggested that A. fenestralis and A. lateralis were more likely to engage in typical external fertilization. The adoption of eggs and their effect on female mate‐choice patterns appearred to reduce the importance of certainty of paternity in these species, and probably increased the evolutionary stability of male parental care.     

Prevalence of different modes of parental care in birds

Estimates of the incidence of major classes of parental care by birds are drawn from classical studies that preceded both the publication of a massive secondary literature and the revolution driven by molecular approaches to avian phylogeny. Here, I review this literature in the light of new phylogenetic hypotheses and estimate the prevalence of six distinct modes of care: use of geothermal heat to incubate eggs, brood parasitism, male only care, female only care, biparental care and cooperative breeding. Female only care and cooperative breeding are more common than has previously been recognized, occurring in 8 and 9% of species, respectively. Biparental care by a pair-bonded male and female is the most common pattern of care but at 81% of species, the pattern is less common than once believed. I identify several problems with existing hypotheses for the evolution of parental care and highlight a number of poorly understood contrasts which, once resolved, should help elucidate avian social evolution.     

Evolutionary transitions in parental care in cichlid fish

Cichlid fishes (Cichlidae) are well suited for testing theories of the evolution of vertebrate parental care. These freshwater teleost fish provide parental care for their offspring, display many different forms of care and have interspecific variation in which sex stays with the young. Here, we assemble the first family-wide composite phylogeny based on morphological and molecular studies, and trace two sets of character evolution: form of care (substrate guarding and mouthbrooding), and sex of care-giver (biparental, female-only, and male-only). Mouthbrooding has evolved from ancestral substrate guarding with 10 to 14 transitions and 0 to 3 reversals. The data support hypothesized transitions in the sex of care-giver, with uniparental female care having arisen from biparental care 21 to 30 times with 0 to 10 reversals. There is also evidence that male-only care evolved once from biparental care. These transitions in parental care characters are the most numerous reported for any family of vertebrates and, to our knowledge, provide the first quantitative support for models of parental care evolution in fish.     

Effect of parental care and aggregation on population dynamics

Behavioral changes of animal species can influence the consequence of population dynamics. One of the most remarkable behaviors of animal species is the aggregation by which species can reduce predation risk as a consequence of dilution or the other effects by forming a group. Empirical studies have demonstrated that an incompatibility exists in aggregation since resource competition might become severe at the cost of reducing predation pressure from predatory species. Parental care by supplying the food consumed by adults to their juveniles would reduce the mortality of juvenile due to starvation, but it would reduce the reproduction rate at the same time. In this paper, we study a class of stage-structured resource-consumer models to investigate the effect of behavioral changes on population dynamics. It is shown that under the presence of trade-off in parental care, moderate degrees of parental care will be favored as maximizing the equilibrium density of consumers. For consumer species having a long maturation period, consumer species might get benefit from dilution effects as a result of aggregation despite the elevated resource competition. Aggregation gives rise to two different outcomes in consumer extinction. Resource exhaustion as a consequence of over-exploitation can induce extinction of consumers due to Allee effects if aggregation strongly mediates juvenile survival.     

Costs and benefits of parental care in eastern kingbirds

We manipulated brood sizes of eastern kingbirds (Tyrannus tyrannus)to measure the costs and benefits of parental care and to testwhether kingbirds showed evidence of individual optimizationof reproductive effort. We found that the number of feedingtrips (trips/h) increased and that per capita feeding rates(trips/nestling/h) declined as brood size increased. The declinein per capita feeding rates was mostly due to high feeding rateto broods of one: parents made roughly equal number of tripsto feed each nestling in broods of two to five. Nonetheless,nestling mass declined with brood size, probably because largebroods were fed more small prey. Nestling condition (mass adjustedfor structural size) differed only between broods of one andfive. After controlling for effects of brood size, feeding rateshad no supplementary influence on either nestling size or condition,but productivity and feeding rate were positively and significantlyrelated. Adult male condition did not vary with brood size,manipulated brood size, or total feeding rate, but declinedas the pair's per capita feeding rates increased. In addition,males that returned to breed were in better condition beforeleaving for migration than those that failed to return. Femalecondition tended to decline, and the probability of returningto breed dropped when broods were enlarged. However, femalecondition was independent of the probability of returning. Ourresults show that high feeding rates were costly, but that theycarried benefits (greater productivity). Some evidence for individualoptimization of reproductive effort existed: variability innestling and adult female condition were better explained bychanges in brood size than by the actual number of young inthe nest. However, most evidence supported the alternative thatincreased brood size was equally costly for all birds