Cues for investment: nest desertion in response to partial clutch depredation in dabbling ducks

Parents may use several cues to assess offspring value; however, most studies of parental care have examined only one or a few cues, and often in just a single species. This approach has produced conflicting results, with limited generality, and it remains unclear which cues animals use to adjust parental care. We examined nest desertion in response to natural clutch reductions by predators to determine which of several cues female dabbling ducks use to assess offspring value. Of 3562 duck nests monitored between 1996 and 2001, 30.5% of clutches were partially depredated, of which females deserted 37.7%. Mallard, Anas platyrhynchos (N=754) and gadwall, A. strepera (N=221) females were more likely to stay with proportionately larger remaining clutch sizes, older clutches and nests with eggs missing rather than with eggshell evidence of depredation. The proportion of the clutch remaining had the greatest influence on the likelihood that a nest would be deserted, indicating that females assess clutch value primarily using the remaining clutch size relative to the initial clutch size. On average, females deserted nests when 37-45% of the clutch remained (3-4 eggs) and continued to provide care when 73-75% of the clutch remained (6-7 eggs). Nest initiation date was not an important cue influencing desertion. Northern pintail, A. acuta (N=33) females behaved similarly, although we could not determine which of several cues relating to clutch size they used because multiple models fit the data well. Our results indicate that several factors influence clutch value and that ducks are able to use multiple cues to finely adjust their level of parental care following partial clutch depredation.Copyright 2003 The Association for the Study of Animal Behaviour. Published by Elsevier Ltd. All rights reserved.     

Nest Crypsis, Reproductive Value of a Clutch and Escape Decisions in Incubating Female Mallards Anas platyrhynchos

In cryptically coloured birds, remaining on the nest despite predator approach (risk‐taking) may decrease the likelihood that the nest will be detected and current reproductive attempt lost. By contrast, flushing may immediately reveal the nest location to the predator. Escape decisions of incubating parents should therefore be optimized based on the risk‐to‐parent/cost of escape equilibrium. Animal prey may assess predation risk depending on a variety of cues, including the camouflage that vegetation provides against the predator. We examined interactive effects of nest crypsis and the current reproductive value of a clutch on flushing distances in incubating mallards (Anas platyrhynchos) approached by a human. Our results were consistent with predictions of parental investment theory: flushing distances were inversely correlated with measures of the reproductive value of the current clutch, namely with clutch size, stage of incubation and mean egg volume. Independently of a reproductive value of a clutch, nest concealment explained a significant portion of the variation in flushing distance among females; individual females tended to increase/decrease flushing distances according to change in nest cover. The results further suggest that vegetation concealment greatly influenced the risk of nest detection by local predators, suggesting that vegetation may act as a protective cover for incubating female. A female's ability to delay flushes according to the actual vegetation cover might thus be viewed as an antipredator strategy that reduces premature nest advertising to visually oriented predators. We argue, however, that shorter flying distances from densely covered sites might be maladaptive in areas where a predator's ability to detect incubating female does not rely on visual cues of nests.     

Nest shape explains variation in sexual dichromatism in New World blackbirds

Following Charles Darwin, research on sexual dichromatism has long focused on sexual selection driving ornamentation in males. However, Alfred Russel Wallace proposed another explanation – that dichromatism evolves as a result of selection favoring crypsis in incubating females. Many recent studies suggest that evolutionary changes in sexual dichromatism often result from changes in female, in addition to male, plumage, yet the evolutionary mechanisms driving changes in female plumage remain largely unexplained. To test Wallace's hypothesis, we examined variation in sexual dichromatism and nest shape, a proxy for predation risk, among New World blackbirds (Aves: Icteridae). Phylogenetic models reveal an evolutionary correlation between sexual dichromatism and nest exposure. Specifically, we found that transitions in monochromatic lineages with exposed nests toward either concealed nests or dichromatism were common. Although this evidence supports Wallace's hypothesis that female incubation leads to selection for crypsis or concealment, we also found that transitions to monomorphism were common, even in lineages with exposed nests – a result suggestive of a role for positive selection on female ornamentation. These patterns of plumage evolution support a growing body of work emphasizing the importance of developing and testing hypotheses to explain evolutionary changes in female, as well as male, ornamentation.     

Mutual ornamentation and the parental behaviour of male and female Collared Flycatchers Ficedula albicollis during incubation

One of the benefits of mate choice based on sexually selected traits is the greater investment of more ornamented individuals in parental care. The choosy individual can also adjust its parental investment to the sexual signals of its partner. Incubation is an important stage of avian reproduction, but the relationship between behaviour during incubation and mutual ornamentation is unclear. Studying a population of Collared Flycatchers Ficedula albicollis, we monitored the behaviour of both sexes during incubation in relation to their own and their partner's plumage traits, including plumage‐level reflectance attributes and white patch sizes. There was a marginally positive relationship between male feeding rate during incubation and female incubation rate. Female but not male behavioural traits were associated with the laying date of the first egg and clutch size. The behaviour of the two sexes jointly determined the relative hatching speed of clutches and the hatching success of eggs. Females with larger white wing patches spent less time incubating eggs and left the nestbox more frequently. Males with larger white wing patches fed females less frequently, whereas males with brighter white plumage areas visited the nestbox more regularly without feeding. Females tended to leave the nest less often when mated to males with larger wing patches, and females spent less time incubating when males had more UV chromatic plumage. The behaviour of both partners during incubation therefore predicted hatching patterns and was correlated with their own and sometimes with their partner's plumage ornamentation. These results call for further studies of mutual ornamentation and reproductive effort during incubation.     

Reversed sexual size dimorphism and parental care in the Red-footed Booby Sula sula

The 'division-of-labour' hypothesis predicts that males and females perform different roles in parental care and that natural selection acts differently on each sex so as to produce different body size optima suited to their particular roles. Reversed sexual size dimorphism in avian species (females larger than males) may therefore be an adaptive consequence of different roles of males and females in parental care. We investigated patterns of nest attendance, brooding, foraging and provisioning rate in a tropical seabird, the Red-footed Booby Sula sula , a species showing a reversed sexual size dimorphism. During incubation, females attended the nest more often than males, and spent more time brooding the small chick than did males during daytime. Males and females did not differ in the average duration of their foraging trips. During incubation, there was a positive relationship between nest attendance and the duration of foraging trips in males, but not in females. During the small-chick stage, for the same time spent at the nest, males spent significantly more time than females at sea. On average, females fed the chick more often than did males. In males, there was a significant and positive relationship between the probability of feeding the chick and the duration of the foraging trip, whereas in females, this probability was much less dependent on the duration of the foraging trip. Overall, female Red-footed Boobies achieved slightly, but significantly, more parental commitment than did males. However, these sexual differences in parental participation were small, suggesting a minimal division of labour in the Red-footed Booby. Our results suggest that the division of labour hypothesis is unlikely to explain fully the adult size dimorphism in Red-footed Boobies.     

Broad‐scale variation in sexual dichromatism in songbirds is not explained by sex differences in exposure to predators during incubation

The evolution of sexual dichromatism provoked one of the greatest disagreements between Charles Darwin and Alfred Russel Wallace. According to Darwin the main driving force is sexual selection, whereby choosy females prefer showy males, leading to the evolution of conspicuous male plumage. On the other hand, Wallace suggested that dichromatism may arise because nest predation favors more cryptic females. To test the role of natural selection in the evolution of dichromatism we combined quantitative data on differences in parental share in nest attentiveness (representing the strength of natural selection on males vs females) with spectrophotometric measurements of dichromatism in 412 species of songbirds from 69 families. We expected to find stronger dichromatism in open‐nesting species with more divergent parental roles and in body parts exposed during incubation. Dichromatism was not related to the differences in parental share during incubation, but it was most pronounced in lekking species, migrants, and small species. Our results thus suggest that Wallace's hypothesis is not able to explain broad‐scale variation in the dichromatism of songbirds, but point to a role for sexual selection, mutual mate choice, and migration strategy in shaping the extraordinary variation in dichromatism exhibited by songbirds.     

Parental behaviour in the Lapwing Vanellus vanellus

Parental behaviour of monogamous and polygynous Lapwings was studied during incubation and brood care. Both parents attended the nest in 86% of monogamous pairs ( n = 29 pairs). In 14% of pairs, only the male parent continued incubation until the eggs hatched, whereas the female deserted the clutch before or at the end of incubation. There was a clear division of parental roles during incubation. Females spent more time incubating (64% of time) than their mates (27%), whereas males spent more time defending the nest (3%) than females (>1%). Time spent incubating did not differ between monogamous and polygynous males. However, polygynous females spent more time incubating (primary females: 95%; secondary females: 97%) than monogamous females. Biparental care was the most common pattern of post-hatching care, although in some broods either the male or the female parent deserted before the chicks fledged. Division of sex roles was less pronounced in brood care than during incubation. Females spent more time brooding (21%) than males (3%), and females attended their chicks more closely than males. Nevertheless, males and females spent similar amounts of time defending the brood from predators and conspecifics. We suggest that the apparent division of parental roles may be explained by sexual selection, i.e. the remating opportunities for male Lapwings might be reduced if they increase their share in incubation. However, the different efficiency of care provision, for example in ability to defend offspring, may also influence the roles of the sexes in parental care.     

Sex-specific defence behaviour against brood parasitism in a host with female-only incubation

Nest protection against intruders is an indispensable component of avian parental care. In species with biparental care, both mates should evolve nest defence behaviour to increase their reproductive success. In most host-parasite systems, host females are predicted to have more important roles in nest defence against brood parasites, because they typically are primarily responsible for clutch incubation. Male antiparasitic behaviour, on the other hand, is often underestimated or even not considered at all. Here we investigated sex-specific roles in four aspects of great reed warbler (Acrocephalus arundinaceus) nest defence against a brood parasite—the cuckoo (Cuculus canorus), namely (1) mobbing, (2) nest attendance/guarding, (3) nest checking and (4) egg ejection. Using dummy experiments, simulating brood parasitism and by video-monitoring of host nests we found that males took the key roles in cuckoo mobbing and nest guarding, while females were responsible for nest checking and egg ejection behaviours. Such partitioning of parental roles may provide a comprehensive clutch protection against brood parasitism.     

Parent birds assess nest predation risk: influence of cavity condition and avian nest predator activity

Skutch hypothesized that nest predators visually assess parental activities to locate a prey nest, whereas parents modify fitness‐related traits to reduce the probability of nest predation. We examined how cavity condition and parental activity interact with avian nest predators to shape the nest success of two coexisting parid species, marsh tits Poecile palustris and oriental tits Parus minor, breeding in nest‐boxes during the incubation period. Nest‐boxes were manipulated to create a prolonged risk of nest predation (entrance diameter 2.6 cm control vs 5.5 cm treatment) soon after clutch completion. To measure changes in parental behavior, we also simultaneously simulated a pulsed risk of nest predation, using sound playbacks of a coexisting control bird and an avian nest predator. We found that the parent tits merely responded the pulsed risk, presumably due to an environment with high avian nest predator encounters, compared to the prolonged risk. Instead, both species spent more time on vigilance at the nest, only under prolonged risk conditions. The activity of corvids near the nest‐box was higher in the marsh tit than that in oriental tits. This activity was also higher in the treatment nest box than that in the control nest‐box. Nest predation during the incubation period was higher in marsh tits than in oriental tits, presumably due to higher and more plastic vigilance in oriental tits, compared to marsh tits. Our results highlight that the differences in cavity condition and parental activities at the nests of two coexisting non‐excavators may contribute to differential nest predation by attracting avian nest predators.     

Evolution of reversed sex roles, sexual size dimorphism, and mating system in coucals (Centropodidae, Aves)

The evolution of greater male than female parental care remains poorly understood. In birds it is thought to be related to precocial chicks and small clutch size. This review shows, however, that such role reversal has also evolved in a family with altricial young and relatively large clutch size: coucals (Centropodidae, Cuculiformes). Males perform most nest building, incubation, and feeding of young. As predicted by sexual selection theory, coucals have also reversed sexual size dimorphism, females being larger than males in all 12 species for which size data are available. Most coucals that have been studied are monogamous, but the black coucal Centropus grillii appears to be polyandrous, and males perform almost all parental care, whereas females show more active advertisement behaviour. In this species, females are about 50% heavier than males. Polyandry in the black coucal seems to be associated with a shift to a habitat with seasonally rich food resources. Difficulties for female coucals of gathering enough resources for producing several clutches of relatively large eggs may favour mainly male parental care. Female sexual competition and resource storage, and male foraging economy, may explain why females are larger. Additional field studies are needed to test these hypotheses; the coucals are of great interest to sexual selection and mating systems theory.     

Experimental manipulation of female tail length did not cause differential allocation by males in the barn swallow

The evolution and maintenance of female ornamentation has attracted increasing attention, because the previous explanation, that is a non‐functional copy of functional male ornamentation, seems insufficient to explain female ornamentation. A post‐mating sexual selection, differential allocation, may be more common than pre‐mating sexual selection, but few studies have investigated differential allocation by males. Here, we studied differential allocation of incubation investment by male barn swallows Hirundo rustica, a model species for the study of sexual selection, because our previous correlative study demonstrated a positive relationship between female tail length and male incubation investment. We manipulated the length of the outermost tail feathers in females after clutch completion and examined whether males adjust incubation investment according to female ornamentation. Because extra‐pair paternity is virtually absent in the study population, we were able to study differential allocation based on the tradeoff between current and future reproductive investments, rather than the tradeoff between current paternal investment and additional mating effort. The experimental treatment had no significant effect on male nest attentiveness, whereas female tail length before manipulation predicted male nest attentiveness. The observed pattern is consistent with differential access; that is, well‐ornamented individuals have greater access to mates with high reproductive (parental) ability, rather than differential allocation during incubation. Alternatively, males can directly assess eggs in their nests, and thus, as seen in other species, males might adjust their incubation investment based on the egg characteristics of long‐tailed females.     

Impaired flight ability during incubation in the pied flycatcher

During the breeding season, many female passerine birds increase in body mass before egg laying, maintain a relatively high body mass during incubation, and then drop back to the original level during the chick-rearing period. The post-hatching reduction in body mass, which can be as large as 10–20%, has been suggested to represent an adaptive mass loss to reduce wing loading, thereby increasing parental flight efficiency when chicks have hatched and have to be fed. Here we present the first study of changes in flight ability from incubation to chick rearing in birds. Wild female pied flycatchers Ficedula hypoleuca flew more slowly during incubation than during chick rearing; a 7% reduction in body mass after the chicks had hatched was associated with a 10% increase in vertical take-off speed. Furthermore, the flight muscle size of the females tracked the reduction in wing load, suggesting that muscle size was adaptively reduced when no longer needed. Since incubation-feeding by males reduces the time females have to spend outside the nest foraging, our results suggest that in addition to increasing female nutritional status and reducing incubation time, incubation-feeding will also reduce predation risk during the period when females face impaired flight ability.     

Predator-induced plasticity in nest visitation rates in the Siberian jay (Perisoreus infaustus)

Bird nestlings may be at risk not only from starvation but alsofrom predators attracted to the nest by parental feeding visits.Hence, parents could trade reduced visitation rates for a lowerpredation risk. Here, through field data and an experiment,we show plasticity in daily patterns of nest visitation in theSiberian jay, Perisoreus infaustus, in response to predatoractivity. In high-risk territories, jay parents avoided goingto the nest at certain times of the day and compensated by allocatingmore feeding effort to periods when predators were less active.Such modifications in provisioning routines allowed parentsin high-risk habitat to significantly lower the risk of providingvisitation cues to visually oriented corvid nest predators.These results indicate that some birds modify their daily nestvisitation patterns as a fourth mechanism to reduce predator-attractingnest visits in addition to the clutch size reduction, maximizationof food load-sizes, and prevention of allofeeding suggestedby Skutch.     

Is Carrying Feathers a Sexually Selected Trait in House Sparrows?

Males in several avian groups carry specialised materials as part of their courtship display. Females may vary their investment in reproduction in relation to their mates' attractiveness. The house sparrow (Passer domesticus) population on Dassen Island, South Africa, builds domed nests in the branches of trees. These nests are more or less spherical structures with a deep cup lined largely with feathers. When males collect feathers, they call to females and display the feather before it is added to the nest. We examined whether carrying feathers provides females with an index of male quality, which correlates with their subsequent investment in parental care. Additionally, we studied the potential importance of feathers in nest insulation. Feathers were collected mainly by males. Males also brought larger feathers, and deposited more feathers in nests, than females. Number of trips with feathers – which increased after feathers were experimentally removed from nests – and number of feathers brought varied among males. Volume of feathers influenced females' investment in reproduction and positively correlated with clutch size and chick feeding rates. We found more feathers during incubation and immediately after chicks hatched, when nest heat requirements peak. Furthermore, number of trips with feathers and number and size of feathers were greater during incubation. Our results suggest that this feather‐carrying behaviour by male house sparrows influences maternal reproduction investment and could be a kind of parental care per se by supplementing nest insulation.     

Video nest monitoring reveals male coloration-dependant nest predation and sex differences in prey size delivery in a bird under high sexual selection

Increased predation risk should select for reduced parental activity to decrease the probability of visually hunting predators discovering the nest. Parental activity and conspicuousness are known to increase predation risk. Here, we test for sex differences in parental visitation rate (number of visits), time seen at the nest (time at the nest × adult visibility), and food delivery (prey size) using continuous video recordings at nests. We test the role of these variables for predation outcome in the Superb Fairy-wren (Malurus cyaneus). The study species is sexually dimorphic: males have iridescent blue plumage while females have brown plumage. The results showed that nest predation was predicted by male time seen at the nest (but not visitation rate), but not female time seen at the nest (or visitation rate). Contrary to our expectation that males would have lower visitation rates than females, our analysis of video images showed that male and female visitation was comparable but that males consistently brought smaller prey items to the nest than females. These findings are discussed in the light of morphological differences between male and female beak size. We conclude that sexual selection has favoured conspicuous male signalling in this system, and that natural selection should select for reduced parental care for the conspicuous sex.     

State-dependent incubation behaviour in the high arctic barnacle geese

Energetic trade-offs between time spent on incubation and times spent on foraging for nesting birds give individuals in good body condition the possibility to incubate more continuously. In the present paper, the incubation behaviour of female barnacle geese Branta leucopsis was quantified in a colony in Svalbard. Females were weighted in early incubation and feeding recess lengths and frequencies were recorded. The feeding behaviour during the course of incubation was significantly correlated to by body mass, and heavy females had both fewer and shorter feeding recesses than lighter females. Moreover, there was an increase in the number of feeding recesses and the total feeding time as the incubation period progressed. Neither clutch size nor egg laying date had an effect on incubation behaviour. However, clutch size was positively related to female body mass suggesting that high-quality females produce large clutches but also allocate more body reserves to incubation. Females left the nest to feed at all times of the day, but more frequently during day time. This was not related to their body mass. Females presumably leave their nest at the time of day when the costs to reheat eggs are at a minimum. The diurnal rhythm may also be adjusted to the activity by egg predators. Overall the results support the state-dependent hypothesis for incubation behaviour, suggesting that body condition at the start of incubation is an important factor for incubation behaviour in barnacle geese.     

Females that experience threat are better teachers

Superb fairy-wren (Malurus cyaneus) females use an incubation call to teach their embryos a vocal password to solicit parental feeding care after hatching. We previously showed that high call rate by the female was correlated with high call similarity in fairy-wren chicks, but not in cuckoo chicks, and that parent birds more often fed chicks with high call similarity. Hosts should be selected to increase their defence behaviour when the risk of brood parasitism is highest, such as when cuckoos are present in the area. Therefore, we experimentally test whether hosts increase call rate to embryos in the presence of a singing Horsfield''s bronze-cuckoo (Chalcites basalis). Female fairy-wrens increased incubation call rate when we experimentally broadcast cuckoo song near the nest. Embryos had higher call similarity when females had higher incubation call rate. We interpret the findings of increased call rate as increased teaching effort in response to a signal of threat.     

State-dependent incubation behaviour in the zebra finch

State dependence is thought to be an important factor in resource allocation decisions, particularly in those decisions relating to parental care. Incubation behaviour is a costly part of avian parental care, and therefore likely to depend on the parent's body condition. We manipulated the body condition of zebra finches, Taeniopygia guttata, during incubation by using prelaying diets of different protein content, and induced birds to lay a similar number of eggs. We tested the hypothesis that birds in better body condition would invest more in incubation than birds in poorer condition when incubating on the same diet. Females that had received a high-protein prelaying diet lost more body mass than those that had received a low-protein diet. They also increased the length of their incubation bouts between early and middle incubation, whereas females that had received a low-protein prelaying diet increased bout length only between middle and late incubation. There were no differences between males from the two diet groups, and males were responsible for a lesser proportion of incubation than females. These results indicate that incubation behaviour is state dependent in female zebra finches, and that birds of different body condition adopt different incubation strategies. We found no differences in incubation duration and hatching success between the two incubation strategies in captivity, but the potential risk of nest predation in the wild may differ. We suggest that only females in good condition can afford to adopt a strategy of increasing bout length early in incubation; females in poorer condition first have to recover their body condition after having produced a clutch. Copyright 2003 Published by Elsevier Science Ltd on behalf of The Association for the Study of Animal Behaviour       

Nest size affects clutch size and the start of incubation in magpies: an experimental study

Nest size has been suggested to be a sexually selected traitindicating parental ability of both males and females. To testwhether a female's reproductive decisions (e.g., clutch sizeand starting incubation) change in relation to experimentalmanipulation of nest size, as would be predicted if nest sizeis a sexually selected signal reflecting the male's parental quality, we manipulated nest size in a population of monogamousmagpies before laying by adding or removing about 20 cm oflarge sticks in the roof of magpie nests. On the one hand,we found that clutch size of reduced nests was smaller thanthat of control or enlarged nests. Moreover, clutch size was significantly related to nest size after manipulation, whichindicates that females adjust clutch size to the final sizeof the nest, nest size thereby being a good candidate for asexually selected trait. On the other hand, number of eggshatched during the first day is hypothesized to be related to the expected available resources during nestling growth, andsubsequent nestlings hatched are likely to die due to broodreduction if resources are not sufficient to raise well-developednestlings. Nest size is hypothesized to inform females abouta male's willingness to invest in reproduction, and we foundthat in broods of experimentally reduced nests, females startedto incubate earlier in the laying sequence than they did inbroods of control or enlarged nests. Moreover, in experimentallyreduced nests, fewer nestlings hatched during the first day,and the difference in body mass between the first and the fourthnestling hatched increased. This result is in accordance withthe hypothesis that the female's decision of when to start incubationin the laying sequence is mediated by nest size, a sexuallyselected trait signaling parental quality. We discuss alternativeexplanations for the results such as the possibility that nestsof different treatments may differ in their thermoregulationproperties or in their protection against predators.     

Comparative manipulation of predation risk in incubating birds reveals variability in the plasticity of responses

The evolution of different parental care strategies is thoughtto result from variation in trade-offs between the costs andbenefits associated with providing care. However, changingenvironmental conditions can alter such fitness trade-offsand favor plasticity in the type or amount of parental care provided. Avian incubation is a form of parental care whereparents face changing environmental conditions, including variationin the risk of nest predation. Because parental activity candraw attention to the location of the nest, a reduction innest visitation rates is a predicted response to an increased,immediate predation risk. Here, we experimentally increasedthe risk of nest predation using model presentations at nestsof five coexisting species that differ in their ambient levelsof nest predation. We examined whether individuals detect changesin nest predation risk and respond by reducing visitation tothe nest. We also tested whether this behavioral response differsamong species relative to differences in their ambient risk of nest predation. We found that males of all species detectedthe increased predation risk and reduced the rate at whichthey visited the nest to feed incubating females, and the magnitudeof this change was highly correlated with differences in therisk of nest predation across species. Hence, as the vulnerabilityto nest predation increases, males appear more willing to trade the cost of reduced food delivery to the female against thebenefit of reduced predation risk. Our results therefore suggestthat nest predators can have differential effects on parentalbehaviors across species. We discuss how the comparative natureof our results can also provide insight into the evolution of behavioral plasticity.