Common goldeneyes adjust maternal effort in relation to prior brood success and not current brood size

Parental investment theory predicts that parental effort should be related to the reproductive value of the current brood. This depends on both the number of young and the survival prospects of each of them. Thus parents may provide more care to larger broods either because of (1) the direct effect of brood size per se on reproductive value (the “brood size” hypothesis) or because (2) past mortality, reflected in current brood size, predicts future mortality of the brood and hence its reproductive value (the “brood success” hypothesis). Earlier studies have not attempted to distinguish between these alternatives. We tested the hypotheses in the precocial, nidifugous common goldeneye Bucephala clangula, a species with uniparental female care. Maternal effort was measured as the time spent by the female in rearing the brood. We found that brood size itself is not associated with maternal effort, but that females modify their maternal effort according to the mortality already experienced by the brood, supporting the prediction of the brood success hypothesis. We also found that brood mortality varied considerably between broods and that previous mortality predicts future mortality within broods, basic assumptions of the brood success hypothesis. Received: 30 January 1996 / Accepted after revision: 27 October 1996     

Parental effort in the California gull: tests of parent-offspring conflict theory

Summary Parental effort was studied among knownaged California gulls (Larus californicus) with a brood size of two. Results supported three of Triver's predictions from parent-offspring conflict theory. First, the amount of time parents withheld food from offspring increased with increasing offspring age. Second, older parents were less likely than younger parents to withhold food from offspring throughout the period of parental care. Third, older parents had a longer period of parental care compared to younger parents. Adult survival to future breeding seasons was inversely related to duration of parental care. Older parents, in association with their greater levels of parental effort, had a lower survival rate compared to that of younger parents.     

Determinants of parental effort: a behavioural study in the Eurasian kestrel,Falco tinnunculus

We recorded behaviour of kestrels (Falco tinnunculus) in western Finland during the courtship (1988–1992), incubation (1989–1991), early nestling (age of young 1–2 weeks, 1989–1992) and late nestling stages (3–4 weeks, 1989–1991) to examine determinants of their parental effort (PE). In males, PE was estimated as the hunting effort (the proportion of budget time spent in flight-hunting) and in females as the food provisioning rate (number of prey items delivered to the nest per hour). The following predictions derived from the parental investment theory were examined. (1) Parents rearing large clutches and broods should invest more in breeding than do parents rearing small clutches and broods. The hunting effort of parents did not increase with clutch or brood size, but males tending large broods had a higher prey delivery rate than males tending small broods (Figs 1–2). (2) PE of parents should increase in the course of the breeding season. In males, this was true only between the incubation and early nestling phases (Fig. 3). (3) The early pairs should invest more in breeding than late ones. This tended to be true during the early (for males) and late nestling phases (for females) (Fig. 4). (4) There should be a negative correlation between PE of mates within pairs, but no evidence for such adjustment was found (Fig. 5). (5) Females mated with bright-coloured attractive males should show higher PE than females mated with dull-coloured males but our results were inconsistent with this prediction. We conclude that PE decisions of kestrels are mainly based on cost-benefit estimates of residual reproductive value, rather than on current investment indicators, like clutch or brood size. This might be beneficial in environments with highly variable survival prospects of offspring caused by pronounced among-year variation in abundance of the main food (microtine rodents). The results also show that hypotheses explaining variation in PE in the short term are not necessarily valid for long-term PE, e.g. tending clutches or broods, which also reflects the demands of female and young.     

Rising costs of care make spiny chromis discerning parents

When the costs of parental care do not scale with the number of offspring being cared for, inclusion of non-descendant young into broods can be advantageous, leading to systems of alloparental care. However, if the cost of care scales with the number of offspring, selection may act against misdirected parental care. The spiny chromis, Acanthochromis polyacanthus, is a marine fish with extended biparental care, and broods that increase in size over the care period strongly suggest that alloparental care occurs in this species. However, A. polyacanthus parents directly provision their offspring by producing ectodermal mucus for their fry to feed on. The costs of such provisioning may scale with brood size, potentially increasing the costs of parental care. Using wild A. polyacanthus pairs, we tested whether foreign offspring are accepted into established broods, and measured how brood defence effort and mucal feeding scale with brood size. We found that A. polyacanthus discriminate between their own and foreign young, vigorously expelling experimentally introduced foreign offspring. Although defensive effort did not scale with brood size, mucal feeding was strongly dependent on brood size, and this increasing cost of care likely acts as the primary selective force on parental discrimination and rejection of foreign fry in A. polyacanthus.     

Competition with flies promotes communal breeding in the burying beetle,Nicrophorus tomentosus

Communal breeding through nest-sharing may benefit cooperating individuals indirectly, in increased inclusive fitness, or directly, when environmental constraints reduce the fitness of solitary breeders. Burying beetles provide extensive parental care and can breed either in pairs or in larger groups of unrelated males and females. Parentage of communally-reared broods is usually shared but is skewed in favor of the individuals of each sex that provide longer care. Females provide care longer than males, and two females are more likely to remain together in the brood chamber than two males are. Flies and other burying beetles are the major competitors for carcasses and this study suggests that it is competition with flies that promotes communal breeding inNicrophorus tomentosus On medium-size carcasses (35–40 g) the presence or absence of oviposition by flies had a significant effect on the size of the brood reared, and on large carcasses (55–60 g) the number of beetles present, two or four, had a significant effect on brood size. On both medium and large carcasses, pairs rearing broods on flyblown carcasses had fewer young than pairs on clean carcasses or foursomes on flyblown carcasses. There was a strong trend for an interaction effect between number of beetles and competition with flies (Table 1). Duration of parental care was not affected by competition with flies except for that of the first male to depart, which provided care longer on flyblown carcasses (Table 2). Pairs and foursomes were equally able to defend the carcass and brood from conspecific intruders and from larger intrudingNicrophorus orbicollis (Table 3).     

Carry-over effects of male extra-pair copulation opportunity on biparental effort in zebra finches

Whether parental effort can be negotiated between partners over ecological time and adjusted across different contexts is not well understood. We manipulated male extra-pair copulation (EPC) opportunity in captive zebra finches, Taeniopygia guttata, to test whether males adjust incubation effort to the mating context and to examine how females respond to their partner’s effort. Birds without previous breeding experience were paired randomly and bred with the same partner twice. In the first breeding attempt, half the males received EPC opportunities with ‘extra-pair females’ during incubation, while the other half did not. Males that received EPC opportunities in the first breeding attempt did not in the second breeding attempt and vice versa. We recorded incubation effort on days when EPC opportunities were not presented. In their first breeding attempt, males with EPC opportunities incubated less than those without. Females compensated fully for the deficit in male care so that a pair’s combined incubation effort was unchanged. In the second attempt, when a male’s opportunity for EPCs was switched, individuals showed the same level of incubation effort that they had previously, irrespective of the current availability of extra-pair females. This suggests that division of effort was negotiated in the first breeding attempt and maintained without significant adjustments in the second attempt. The effects of male EPC opportunity in the first breeding attempt on subsequent incubation effort suggests that individual parental decisions can be shaped by previous experience and this may partly explain conflicting results in studies where individuals’ histories were not known.     

Brood reduction in response to manipulated brood sizes in the common swift (Apus apus)

Following a brood size manipulation experiment on the common swift (Apus apus) in which different levels of parental effort were created, brood reduction occurred in all five nests manipulated to four chicks and in two of the five manipulated to three young. This provided an opportunity for looking in detail at the parental investment decisions concerning allocation strategies between parent and young during the process of brood reduction. The data recorded here were analysed on a visit-by-visit basis regarding changes in parental and chick body masses, the mass of prey delivered and the estimated mass of parental self-feeding. The results show that food delivery rates did not increase in proportion to the number of chicks in the broods. This reduction in delivery rates per chick resulted in lower chick masses and ultimately in the death of one or more chicks in the larger broods. The resulting low parental body masses for adult birds feeding larger broods suggested that these parents could not have raised all their young without risking their own survival. There was a tendency for parents from nests that experienced brood reduction to feed themselves instead of allocating most of the food gathered to the young. After brood reduction, parents regained lost body mass and their young fledged at masses only slightly lower than normal. The differential allocation decisions regarding parental self-feeding which resulted in brood reduction were largely responsible for keeping the parents in good enough condition to care for the surviving nestlings. Therefore, this study clearly demonstrates that brood reduction can operate through the differential allocation of food between parent and young in a way that can have adaptive consequences for the survival of parents and their young. Correspondence to: T.L.F. Martins     

Parental investment decision rules: a test in bluegill sunfish

Summary We review parental investment decision theory and provide an experimental test of the decision rule used by male bluegill sunfish (Lepomis macrochirus) in allocating parental investment to their young. The alternative decision rules tested are: (1) invest according to brood size (number) only; (2) invest according to past investment only; (3) invest according to both brood size and past investment; and (4) invest according to neither brood size nor past investment. By manipulating brood size independently of a male's cumulative investment in the brood, and by measuring each male's defensive behavior against a model predator, we found that male bluegill invest according to both brood size and past investment. This result is consistent with recent theory that past parental investment devalues adult future reproductive value, and that animals should therefore invest according to the value of their brood relative to that of their own expected future reproduction.     

Sex and status in a cooperative breeding fish: behavior and androgens

Among taxonomically widespread cooperatively breeding vertebrates, those with non-breeding helpers-at-the-nest provide an excellent opportunity to understand the proximate mechanisms underlying care and allocare. In this study, we examined androgen levels in relation to care behavior in a cooperatively breeding cichlid fish, Neolamprologus pulcher, from Lake Tanganyika. We concentrated on androgens, as these hormones have been linked to the defense behavior, and the defense of young is a common form of parental care in fishes. N. pulcher dominant female breeders performed the most care and also displayed the highest levels of plasma testosterone (T) compared with other individuals within the social group. We also found that dominant male breeders provided a similar amount of care as did the subordinate helpers, but breeding males had the highest levels of 11-ketotestosterone (11KT), an important androgen in fish. Breeders had higher levels of both androgens (T and 11KT) compared to helpers. There was a weak but significant positive correlation between T levels and the frequency of care regardless of sex and status. Our results suggest that androgens may promote defense of young and are in contrast to the commonly reported trade-off between androgen and parental care.     

Differential effects of offspring condition-dependent signals on maternal care regulation in the European earwig

Parent–offspring conflict theory predicts the evolution of offspring solicitation signals that can influence the amount and/or the duration of parental investment. Short-term effects of offspring solicitation signals on parental food provisioning have been widely demonstrated, but persistent effects of offspring signals on the maintenance of parental care have been rarely studied. Also, the relation between the amount of care provided to the brood and how it is distributed among individual offspring within a brood is not well enough understood. Here, we investigated in the European earwig (Forficula auricularia) the effects of offspring condition-dependent chemical signals on the maintenance of maternal care among broods and the distribution of maternal food within broods. Mothers were isolated from their brood for 3 days and continuously exposed to chemical signals extracted from broods of experimentally manipulated nutritional state. After re-introducing mothers to their brood, a range of maternal behaviours were quantified. We found that earwig mothers groomed their offspring significantly more after exposure to chemical extract from high-food brood in comparison with mothers exposed to extract from low-food brood, which in turn displayed significantly more aggressive behaviour. Furthermore, we manipulated offspring individual nutritional condition within the brood to evaluate the effect of offspring state on the within-brood food distribution. Within broods, poorly fed individuals received significantly more food than well-fed individuals, probably due to scramble competition. These results show that earwig nymphs express multi-component condition-dependent signals and behaviours differentially affecting maternal care provisioned to the brood and the distribution of care within broods.     

Territory takeover and sexually selected infanticide in tropical house wrens

Summary Tropical house wrens in lowland central Panama are, with rare exception, permanently monogamous. During a 3-year demographic study of 54–56 pairs of these brids, both males and females committed infanticide in association with takeover of breeding territories. New males and new females replaced previously identified (color-banded) parents before the termination of parental care in 13% of 328 breeding attempts. Replacement was accomplished by physical takeover in at least some if not all cases. Total nest failure at the egg, nestling, or fledgling stage occurred in 73% of the male replacements and 70% of the female replacements. Nest predation was excluded as a possible cause of nest failure. 76% of male replacements and 50% of female replacements bred in the same season. Infanticidal replacement males bred sooner than did non-infanticidal males arriving at similar stages of the nesting cycle. Contexts in which infanticide occurred included takeovers by first-year males and females of territories and mates, re-entry into the breeding population by males that had recently lost their mates, acquisition of neighboring females by bigamous males, and the elimination of one female of a bigamous male by the other. Sexually selected infanticide in these birds is promoted by a lengthy breeding season and extremely limited breeding opportunities for individuals not already part of the breeding population. Mate limitation appears to be more important than habitat or nestsite limitation in restricting new breeding opportunities once the breeding season has begun.     

Adjustment of brood care behaviour in the absence of a mate in two species of Nicaraguan crater lake cichlids

In many taxa, parental strategies can vary among individuals. This is especially true in species with biparental care, with males, more often than females, deserting their mates. While there is an abundance of theoretical predictions and empirical data on factors inducing mate abandonment by males, much less is known about what consequences this may have on female behaviour, particularly in the field and in non-avian systems. Here, we compared brood defence rate, behavioural defence types, and brood success of solitary and paired females in two species of Neotropical cichlid fish in their natural habitat. In terms of the rate of territorial aggression towards potential brood predators, solitary females were able to fully compensate in the absence of a male but, in so doing, ended up maintaining smaller territories, which appeared to compromise offspring fitness in at least one of the two species. Hence, our results suggest that even extensive quantitative compensation in parental effort by solitary females may not be enough to ensure adequate qualitative compensation for the lack of male participation, highlighting the importance of distinguishing between these two aspects of compensatory parental care.     

Is reduced clutch size a cost of parental care in Eastern Phoebes (Sayornis phoebe)?

What is the cost of parental care in birds? Previous studies using observational and experimental techniques on nest building and clutch sizes in a small migrant flycatcher, the Eastern Phoebe (Sayornis phoebe), led to contradictory results that did not show a consistent cost of current reproductive effort on residual reproductive output. The data presented here indicate that different elements of parental behaviors are indeed costly because they reduce various aspects of phoebes' subsequent reproductive performance. Experimental removal of old nesting structures at previously used breeding sites reduced but did not eliminate the chance of phoebes' settlement in the subsequent year. Comparing sites at which phoebes did and did not build new nests showed that nest builders completed their first clutches later, had lower probabilities of second breeding attempts, and more often lost their nesting attempt due to fallen nest structures than nest reusers. There was, however, no significant effect of nest building on the clutch sizes and rates of cowbird parasitism of first nesting attempts. Overall, sites with newly built nests had lower seasonal reproductive effort than sites with reused nests. I also examined phoebes' relative residual reproductive output in a separate breeding season when nest building was not experimentally manipulated. When controlled for confounding variables this analysis indicated that in those phoebes that did breed for a second time, the relative decrease of the sizes of first to presumed second clutches was greater at sites where first breeding attempts consisted of more total nestlings. These data are consistent with the hypothesis that parental care is costly in Eastern Phoebes and support predictions of trade-offs between the nest building, brood care, and residual egg-investment components of reproduction.     

Parentage and paternal care: consequences of intersexual selection in Savannah sparrows?

Empirical relationships between parentage and male parental care are commonly interpreted in the context of life-history models that consider increased offspring survivorship as the only benefit of paternal effort. However, indirect benefits associated with male care can also influence a male's response to cuckoldry: if females allocate paternity according to their prior experience with male parental care, it may pay for males to provision extra-pair young in early broods. Here, I assess the relationship between first-brood parentage and paternal care in a population of Savannah sparrows (Passerculussandwichensis) where a male's fertilization success in the second brood appears to be influenced by his prior parental performance. Based on the multi-locus DNA fingerprinting of 17 first broods, male feeding effort was influenced by parentage (percent of brood resulting from within-pair fertilizations) but not by brood size, male mating status (monogamous versus polygynous), timing of breeding (hatching date), structural size (wing length) or condition (mass). Males provided more care to broods that contained few within-pair young. This result supports the idea that males provision young to increase their future mating success, but alternative hypotheses involving male quality and timing of breeding cannot be excluded. Received: 13 August 1996 / Accepted after revision: 22 February 1997     

Manipulation of sex differences in parental care

Summary In a species with biparental care two parents cooperate to provide the appropriate amount of care for the young. Recent theoretical treatments consider the evolutionarily stable investment strategy. Under most conditions, the parental investment of the two partners should be negatively correlated, with the shortfall of one partner being partially compensated for by the other. Previous experimental manipulations of biparental care have involved removal of one partner, yet the response of a widowed bird may differ from that of a mated bird whose partner is doing less than its fair share of parental care. We present the first data involving subtle manipulations of sex differences in parental care where both partners continue to care for the young. This study involves pairs in a nestbox colony of european starlings (Sturnus vulgaris L.) with all brood sizes manipulated to five chicks. Pairs were randomly assigned to three groups: (i) male parental care reduced; (ii) female parental care reduce; and (iii) control pairs. Parental care was manipulated by attaching small weights to the base of a bird's tail feathers. Regardless of sex, nest visitation rate was reduced in the weighted birds with an incomplete compensatory increase by their unweighted partner. Additional parental duties were also considered, including shifts in prey type delivered to the nest, in both weighted birds and their partners. The shift in diet and the overall lower total visitation rate in experimental nests contributed to slower chick growth and lower chick weights than in control nests. The data accord with models suggesting that equality of invesment in biparental species is evolutionarily stable, but reveal new dimensions of parental response that need to be taken into account in theoretical treatments.     

Brood dispersal and multiple central place foraging by Lapland longspur parents

Summary Lapland longspur chicks continued to be fed by their parents for 2 weeks after nest departure. Shortly after they left the nest, broods were divided evenly into two units each tended by a single parent. Female-tended brood units dispersed away from the nest at a faster average distance per day than those tended by males. The distance between offspring within a brood unit also increased as chicks got older. For the first 8–10 d after nest departure, parents were multiple central place foragers, making 1–8 foraging trips away from each dispersed chick (i.e. the central place) before moving on to feed another chick in a similar fashion. During the final 5–7 d before independence, chicks were quite mobile and followed parents on their foraging bouts. A simulation model shows that brood dispersal reduced total parental travel time per chick, primarily because each chick moved closer to a foraging site. By comparing models for a variety of brood division and foraging itinerary scenarios, we also show that multiple central place foraging by parents visiting different, separated brood units is less energetically expensive than other reasonable alternatives.Although brood dispersal is usually considered to be an adaptation for avoiding predation, it can also help parents reduce the energetic costs of parental care.     

Parental investment and pair-bond behavior among canvasback ducks (Aythya valisineria,Anatidae)

Summary Hypothetical patterns of male and female cumulative reproductive effort in canvasback ducks were used to predict the efforts of males and females in pair-bond reinforcing behavior through a breeding sequence. The predictions were that, at any point in time in a monogamous breeding system, given certain assumptions, (a) the sex investing less should be more active in reinforcing the pair bond, and (b) this relationship should shift within and between breeding attempts with the pattern of cumulative reproductive effort per brood by the male and female. Data on the behavior of newly-formed pairs were obtained by observing apparently paired but unmarked canvasbacks during spring migration. Later, 11 individuallymarked pairs were followed through breeding sequences, including repeated nesting attempts. Observed affiliative behavior fit the predictions reasonably well. That sex whose cumulative reproductive effort was less tended to be more active in maintaining proximity to its mate, initiating bouts of mutual display, and coordinating pair activities. Predictions were met in 14 of 24 cases, results were contrary in 3 cases, and in 7 cases trends were not statistically different (P>0.05). Shifts in relative male and female reinforcement efforts that coincided with major changes in investment were apparent. These results support the proposition that factors other than simple parental investment-related desertion costs might be important to an individual's behavioral decisions regarding pairbond reinforcement and ultimately mate abandonment. Discrepancies in a few predicted outcomes further suggest that males and females may use and balance various pair-reinforcement tactics differently through a breeding season.     

Brood parasitism disproportionately increases nest provisioning and helper recruitment in a cooperatively breeding bird

Obligate avian brood parasites lay their eggs in nests of other species (hosts), which raise parasitic young. Parasitic nestlings are likely to influence host’s parental behaviours as they typically beg for food more vigorously than young host for a given hunger level. However, few studies have tested this idea, with conflicting results. These prior studies were largely limited to biparental hosts, but little is known about the effect of brood parasitism on parental behaviours in hosts that breed cooperatively. We followed a multimodel approach to examine the effect of brood parasitism on nest provisioning and helper recruitment in the baywing (Agelaioides badius), a cooperative breeder parasitised by screaming (Molothrus rufoaxillaris) and shiny (Molothrus bonariensis) cowbirds. Multimodel inference results indicated that feeding visits increased with nestling age, cooperative group size and number of cowbird nestlings in the brood. Brood size had little influence on feeding visits, which further suggests that baywings adjusted their provisioning effort in response to cowbird parasitism. In addition, nests parasitised artificially with shiny cowbird eggs or hatchlings recruited more helpers than unmanipulated nests having only host or screaming cowbird young. Our results provide novel evidence that brood parasitism and cooperative breeding interact in determining the levels of nest provisioning.     

Benefits of large broods by higher chick survival and better territories in a precocial shorebird

When reproductive success is constant in one breeding phase, different tactics that increase variation in reproductive success among individuals may evolve in other phases. For instance, in shorebirds, which usually have a limited clutch size of four eggs, variation in reproductive tactics among individuals is expected either before egg-laying (e.g. diverse mating systems) or after hatching of the young (e.g. diverse parental care). In this paper, I studied the pied avocet (Recurvirostra avosetta), a shorebird with a modal clutch size of four eggs, to test whether post-hatch chick adoption as an alternative tactic can be linked to increased variation in annual reproductive success. When predation was high, naturally adopting pairs produced more filial fledglings than did pairs not adopting chicks and not losing chicks to adoption. The number of filial fledglings increased with the number of adopted young, possibly through diluting the chances of predation on filial young. Experimental chick addition did not lead to more fledged young due to low brood integrity as shown by the frequent loss of chicks from some experimental broods. When predation was low, larger broods occupied feeding territories with higher prey abundance than smaller broods, possibly due to their dominance over smaller ones. Pairs that lost chicks to adoption (donors) fledged as many filial young in their broods as did non-adopters/non-donors, whereas the total number of donors’ filial fledglings, including those raised in adopting broods, approached that of adopters. These findings show, for the first time, that post-hatch alternative reproductive tactics can lead to variation in annual reproductive success and to higher success for some pairs even in species where past adaptations limit variation in reproductive success in a certain phase of reproduction.     

Helpers-at-the-nest have the same provisioning rule as parents: experimental evidence from play-backs of chick begging

Despite the success of kin selection in explaining helping-at-the-nest among communally breeding birds, we know almost nothing about how helpers regulate their chick-feeding effort. This is especially interesting given how much we now know about parental provisioning `rules-of-thumb' and the evolution of chick begging as an honest signal of `need'. This study explores the provisioning rules of helpers and parents in Arabian babblers (Turdoides squamiceps), using tape play-backs to supplement chick-begging signals and increase apparent brood demand. In all eight groups tested, both helpers and parents fed older, noisier broods at higher rates. Total provisioning rates to nests increased during begging play-back days compared to control days. Absolute provisioning rates by helpers and the scale of their responses to play-backs were statistically indistinguishable from those of parents. In both helpers and parents, increases in nest visits during play-backs were associated with reductions in foraging distance from the nest and increases in size of prey delivered. Older birds of both sexes delivered slightly larger prey items, possibly reflecting differences in foraging ability due to experience. These results are consistent with the idea that, like the parents, helpers-at-the-nest in Arabian babblers provision nestlings as part of a strategy of investment, irrespective of helper age, dominance status or sex. In this species, high relatedness within groups may provide parents and helpers with similar kin-selected fitness benefits, although the mutualistic advantages to helpers from simply augmenting group sizes cannot be ruled out. Received: 17 June 1997 / Accepted after revision: 28 February 1998