Differences in parental food allocation rules: evidence for sexual conflict in the blue tit?

Evolutionary conflicts of interest between family members areexpected to influence patterns of parental investment. In altricialbirds, despite providing the same kind of parental care, patternsof investment in different offspring can differ between parents,a situation termed parentally biased favoritism. Previous explanationsfor parentally biased favoritism have received mixed theoreticaland empirical support. Here, we test the prediction that inblue tits, Cyanistes caeruleus, females bias their food allocationrules to favor the smallest offspring during the nestling stage.By doing so, females could increase the subsequent amount ofpaternal care supplied by their partner during the fledgingperiod, as a previous study showed that males feed the largestfledglings. When size differences within the brood are lesspronounced, all offspring will require similar amounts of postfledgingcare, and thus, the male parent will lose the advantage of caringfor the largest offspring that are closest to independence.In this study, we controlled the hunger of the smallest andlargest nestlings in the brood and compared the food allocationrules of the 2 parents. We found that the male parent had astronger preference than the female to feed the closest nestlingsand made no distinction between nestlings based on size, whereasthe female provisioned small hungry nestlings more when theywere at intermediate distances from her. These differences inparental food allocation rules are consistent with predictionsbased on sexual conflict over postfledging parental investment.     

No effect of parental quality or extrapair paternity on brood sex ratio in the blue tit (Parus caeruleus)

Sex allocation theory predicts that parents should manipulatebrood sex ratio in order to maximise the combined reproductivevalue of their progeny. Females mating with high quality malesshould, therefore, be expected to produce brood sex ratiosbiased towards sons, as male offspring would receive a relativelygreater advantage from inheritance of their father's characteristicsthan would their female siblings. Furthermore, it has been suggested that sex allocation in chicks fathered through extrapair fertilizations should also be biased towards sons. Contraryto these predictions, we found no evidence that the distributionof sex ratios in a sample of 1483 chicks from 154 broods ofblue tits (Parus caeruleus) deviated significantly from thatof a binomial distribution around an even sex ratio. In addition,we found no significant effect on brood sex ratio of the individualquality of either parent as indicated by their biometrics, feather mite loads, time of breeding, or parental survival. This suggeststhat females in our population were either unable to manipulateoffspring sex allocation or did not do so because selectionpressures were not strong enough to produce a significant shiftaway from random sex allocation. The paternity of 986 chicks from 103 broods was determined using DNA microsatellite typing.Extrapair males sired 115 chicks (11.7%) from 41 broods (39.8%).There was no significant effect of paternity (within-pair versusextrapair) on the sex of individual offspring. We suggest that,in addition to the weakness of selection pressures, the possiblemechanisms responsible for the allocation of sex may not besufficiently accurate to control offspring sex at the levelof the individual egg.     

Levels of extra‐pair paternity are associated with parental care in penduline tits (Remizidae)

In most passerine birds, individuals attempt to maximize their fitness by providing parental care while also mating outside their pair bond. A sex‐specific trade‐off between these two behaviours is predicted to occur, as the fitness benefits of extra‐pair mating differ between the sexes. We use nest observations and parentage analysis to reveal a negative association between male care and the incidence of extra‐pair paternity across three species of penduline tit (Remizidae). This provides evidence of a trade‐off between these two behaviours, possibly due to the devaluing of paternal care by extra‐pair offspring.     

Effects of nestling condition on UV plumage traits in blue tits: an experimental approach

Intraspecific sexual and social communications are among themost important factors shaping costly color traits in birds.Condition capture models assume that only animals in superiorcondition can develop and maintain a colorful plumage. Althoughthere is good evidence that carotenoid-based components of plumagecolors show condition dependence, the situation is more controversialwith the underlying UV-reflecting structural component. We conducteda brood size manipulation in blue tits (Parus caeruleus) toinvestigate condition-dependent effects on plumage colorationin male and female offspring. Carotenoid chroma and UV reflectanceof the yellow breast plumage showed condition-dependent expressionin male and female fledglings. However, only males that wereraised in reduced broods had higher UV reflectance in the UV/bluetail feathers, whereas female tail coloration did not differbetween treatments. Our data suggest that there is a sex-specificeffect on the blue but not the yellow plumage and that thisis related to differences in the signaling function of bothplumage traits. Although sexual selection may already act onmale nestlings to develop colorful tail feathers for the nextbreeding season, the UV/yellow breast feathers are molted duringthe postjuvenile molt, and their signaling value is likely tobe important for both sexes during the extended postfledglingphase.     

Faithful females receive more help: the extent of male parental care during incubation in relation to extra‐pair paternity in songbirds

Parental care provided by males occurs in a diverse array of animals and there are large differences among species in its extent compared with female care. However, social and ecological factors responsible for interspecific differences in male's share of parental duties remain unclear. Genetic fidelity of females has been long considered important. Theory predicts that females should receive more help from their mates in raising the offspring in species with high genetic fidelity. Using avian incubation behaviour as a model system, we confirmed this prediction. The extent of male's help during incubation increased with decreasing rate of extra‐pair paternity across species (22 species of socially monogamous songbirds from 13 families; male's share of incubation ranged from 6% to 58%), even after accounting for covariates, biases in species selection and intraspecific variability. Moreover, this result was not sensitive to two different phylogenies and branch length estimates. We suggest that our findings support the notion, backed by theory, that genetic fidelity is an important factor in the evolution of male parental care. We offer several behavioural scenarios for the coevolution between male's share of parental duties and the genetic mating system.     

Corticosterone metabolites in blue tit and pied flycatcher droppings: effects of brood size, ectoparasites and temperature

The hypothalamic-pituitary-adrenal (HPA) axis of birds induces the secretion of corticosterone (CORT) as a response to different ecological variables. In this study we tested experimentally if manipulations of brood size or ectoparasitism led to subsequent differences in the concentration of excreted CORT metabolites of adult and nestling blue tits (Cyanistes caeruleus). No significant effect of the manipulation of brood size was detected in adults or nestlings. No significant effect of ectoparasitism was detected in males or nestlings, although females from uninfested nests showed lower concentrations of excreted CORT metabolites. In addition, we analysed if weather conditions had an influence on the concentration of excreted CORT metabolites of blue tits and pied flycatchers (Ficedula hypoleuca) breeding in the same forest. We detected no effect of weather conditions on adults, but nestlings of both species showed a negative correlation between their excreted CORT metabolites and the average mean temperatures they were subjected to during their growth. This effect was not found in blue tits in a colder year, suggesting that the sensitivity of the HPA axis to ambient temperature may be subjected to interannual variation. Moreover, we found a positive effect of the maximum temperature on the day of sampling on the concentration of CORT metabolites of blue tit nestlings in one of the years. These results suggest that weather conditions may act as environmental stressors to which the HPA axis of blue tit and pied flycatcher nestlings may be sensitive.     

Fertilization success and UV ornamentation in blue tits Cyanistes caeruleus: correlational and experimental evidence

Cases where less ornamented males are favored through sexualselection are rare among birds. Here we show, based on datafrom 3 consecutive breeding seasons, that male blue tits withless ultraviolet (UV)-ornamented crown feathers sire more offspring.This pattern was mainly driven by the higher success of older,less UV-ornamented males at siring extrapair offspring. Thereason behind this relationship is unclear although we hypothesizethat being less UV-ornamented may enable adult males to intrudeinto nearby territories by mimicking juveniles. To test causality,we experimentally manipulated male crown coloration creating2 groups, one with higher (UV(+) treatment) and one with lowerUV reflectance (UV(–) treatment). Contrary to our expectations,UV(–) males were less likely to sire extrapair offspringthan UV(+) males. The treatment had no effect on the likelihoodof losing paternity in a male's own nest. Because the experimentalevidence does not support the observational data, a direct effectof male crown color on extrapair success cannot be confirmed.However, potential pitfalls of this and other such color manipulationexperiments, like fading of treatment with time and mismatchesbetween behavior and coloration, call for new improved manipulationtechniques and detailed behavioral observations to conclusivelytest for the effect of blue tit crown coloration on male extrapairsuccess.     

Extra pair paternity in birds: a review of interspecific variation and adaptive function

The application of molecular genetic techniques has revolutionized our view of avian mating systems. Contrary to prior expectations, birds are only very rarely sexually monogamous, with 'extra-pair offspring' found in approximately 90% of species. Even among socially monogamous species, over 11% of offspring are, on average, the result of extra-pair paternity (EPP). Based on over 150 molecular genetic studies of EPP in birds, we review two topical areas: (i) ecological explanations for interspecific variation in the rate of EPP; and (ii) evidence bearing on the adaptive function of EPP. We highlight the remaining challenges of understanding the relative roles of genes and ecology in determining variation between taxa in the rate of extra paternity, and testing for differences between extra-pair offspring and those sired within-pair.     

Correlations between ultraviolet coloration, overwinter survival and offspring sex ratio in the blue tit

We studied the correlations between offspring sex ratio, UV coloration and overwinter survival in a population of blue tits, breeding in Gotland, Sweden, over three consecutive breeding seasons. In 2 of 3 years, we found that females paired to males with relatively brighter UV-coloration produced a greater proportion of sons in their broods, and that this effect was significant with all 3 years combined, despite a significant year by male UV interaction. In addition, we found other correlates of sex ratio (breeding time, female age and clutch size) in some, but not all years, and some of these showed significantly different relationships with sex ratio between years. In both years for which data were available, there were indications that males with relatively brighter UV coloration, and that paired with females that produced male-biased clutches, were more likely to survive to the next year. In addition, we also found that in both males and females, individuals produced similar sex ratios in consecutive years. Because correlations with the sex ratio may be expected to be weak, variation in results between years within the same population may be explained by low statistical power or genuine biological differences. Our results suggest that conclusions about sex ratio variation in birds should be based on multiple years. The correlations that we found in some years of this study are consistent with models of adaptive sex ratio adjustment in response to mate quality. However, careful experimental work is required to provide tests of the assumptions of these models, and should be a priority for future work.     

Within‐population variation in social strategies characterize the social and mating system of an Australian lizard,Egernia whitii

The lizard genus Egernia has been suggested as an excellent model system for examining the evolution of sociality as it exhibits considerable diversity in social organization both between and within species. To date the majority of work examining the factors responsible for the evolution of sociality within Egernia has advocated a broad scale approach; identifying the social structure of specific species or populations and comparing the degree of sociality between them. However, we argue that significant advancements could also be gained by examining variation in social strategies within populations. Here we integrate a detailed, 3‐year, field‐based examination of social spacing and juvenile dispersal with molecular analyses of paternity to determine the social and mating system of a Tasmanian population of White's skink (Egernia whitii). We show that E. whitii live in small stable family groups consisting of an adult male, his female partner(s), as well as juvenile or sub‐adults individuals. In addition, while the mating system is characterized by considerable genetic monogamy, extra‐pair fertilizations are relatively common, with 34% of litters containing offspring sired by males from outside the social group. We also show that traits related to social organization (social group composition, group size, stability and the level of extra‐pair paternity) vary both between and within individuals. We suggest that ecological factors, such as habitat saturation, quality and availability, play a key role in maintaining between individual variation in social strategies, and that examining these individual level processes will allow us to more clearly understand variation in sociality among species.     

High rates of extra‐pair paternity in a socially monogamous beetle with biparental care

1. Nest construction and paternity assurance are predicted to favour biparental care in insects. The horned passalus (Odontotaenius disjunctus) is a socially monogamous beetle with biparental care that breeds in decaying logs. The genetic mating system of the horned passalus was investigated to determine if paternity assurance is likely to drive the evolution or maintenance of paternal care in this system. Parental time budgets were also examined to better understand the types and frequencies of behaviours performed by parents. 2. Genotyping‐by‐sequencing revealed high levels of extra‐pair paternity, with 54.8% of offspring sired by extra‐pair males and 70% of nests containing extra‐pair young. 3. More heterozygous social males were cuckolded less than more homozygous social males. Extra‐pair mating, however, seems unlikely to increase offspring genetic diversity as extra‐pair offspring were not more heterozygous than within‐pair offspring, and average brood heterozygosity did not increase with higher rates of extra‐pair paternity. 4. Behavioural observations demonstrated that parents spent on average 46.5% of their time processing the decaying wood resource for larval offspring. Because resource processing is a by‐product of feeding and provides shareable benefits for all larvae in the brood, this form of paternal care could be favoured despite low paternity.     

Parental investment with a superior alien in the brood

When a parent's parentage differs across breeding attempts, established theory predicts that the parent should invest more in a brood when perceived parentage is high. We present a model of parental investment in which offspring unrelated to the parent have a competitive advantage over the parent's own offspring and take a larger share of investment. We show that this can weaken or, if the competitive advantage is great, reverse the predicted relationship between perceived parentage and parental investment. A moderate competitive advantage of extra-pair young over within-pair young could partly explain the lack of any clear relationship between paternal care and paternity in many studies, and could easily arise if females choose extra-pair partners for good genes. Our results are also relevant to interspecific avian brood parasitism. As parasites reared together with host offspring are often superior competitors, their hosts could benefit from increasing investment in response to suspected parasitism.     

Energy expenditure, nestling age, and brood size: an experimental study of parental behavior in the great tit Parus major

A brood manipulation experiment on great tits Parus major was performedto study the effects of nestling age and brood size on parentalcare and offspring survival. Daily energy expenditure (DEE)of females feeding nestlings of 6 and 12 days of age was measuredusing the doubly-labeled water technique. Females adjusted theirbrooding behavior to the age of the young. The data are consistentwith the idea that brooding behavior was determined primarilyby the thermoregulatory requirements of the brood. Female DEEdid not differ with nestling age; when differences in body masswere controlled for, it was lower during the brooding periodthan later. In enlarged broods, both parents showed significantlyhigher rates of food provisioning to the brood. Female DEE wasaffected by brood size manipulation, and it did not level offwith brood size. There was no significant effect of nestlingage on the relation between DEE and manipulation. Birds wereable to raise a larger brood than the natural brood size, althoughlarger broods suffered from increased nestling mortality ratesduring the peak demand period of the nestlings. Offspring conditionat fledging was negatively affected by brood size manipulation,but recruitment rate per brood was positively related to broodsize, suggesting that the optimal brood size exceeds the naturalbrood size in this population.     

Determinants of distribution and prevalence of avian malaria in blue tit populations across Europe: separating host and parasite effects

Although avian malarial parasites are globally distributed, the factors that affect the geographical distribution and local prevalence of different parasite lineages across host populations or species are still poorly understood. Based on the intense screening of avian malarial parasites in nine European blue tit populations, we studied whether distribution ranges as well as local adaptation, host specialization and phylogenetic relationships can determine the observed prevalences within populations. We found that prevalence differed consistently between parasite lineages and host populations, indicating that the transmission success of parasites is lineage specific but is partly shaped by locality-specific effects. We also found that the lineage-specific estimate of prevalence was related to the distribution range of parasites: lineages found in more host populations were generally more prevalent within these populations. Additionally, parasites with high prevalence that were also widely distributed among blue tit populations were also found to infect more host species. These findings suggest that parasites reaching high local prevalence can also realize wide distribution at a global scale that can have further consequences for host specialization. Although phylogenetic relationships among parasites did not predict prevalence, we detected a close match between a tree based on the geographic distance of the host populations and the parasite phylogenetic tree, implying that neighbouring host populations shared a related parasite fauna.     

The unexpected but understandable dynamics of mating,paternity and paternal care in the ocellated wrasse

Although theory generally predicts that males should reduce paternal care in response to cues that predict increased sperm competition and decreased paternity, empirical patterns are equivocal. Some studies have found the predicted decrease in male care with increased sperm competition, while even more studies report no effect of paternity or sperm competition on male care. Here, we report the first example, to our knowledge, of paternal care increasing with the risk and intensity of sperm competition, in the ocellated wrasse (Symphodus ocellatus). Theory also predicts that if paternal care varies and is important to female fitness, female choice among males and male indicators traits of expected paternal care should evolve. Despite a non-random distribution of mating success among nests, we found no evidence for female choice among parental males. Finally, we document the highest published levels of extra-pair paternity for a species with exclusive and obligate male care: genetic paternity analyses revealed cuckoldry at 100 per cent of nests and 28 per cent of all offspring were not sired by the male caring for them. While not predicted by any existing theory, these unexpected reproductive patterns become understandable if we consider how male and female mating and parental care interact simultaneously in this and probably many other species.     

The function of extrapair paternity in blue tits and great tits: good genes or fertility insurance?

DNA fingerprinting of an island population of blue tits andgreat tits in southeast Norway revealed that extrapair paternityaccounted for 36% (17/47) and 27% (15/55) of broods and for7% (31/466) and 8% (33/408) of young in the two species, respectively.Cuckolded males did not differ from noncuckolded males withrespect to morphology, age, or survival. There was no seasonalpattern in the frequency of extrapair paternity, and males showedno individual consistency in paternity loss over multiple broods.Extrapair offspring did not grow faster, they did not fledgewith a higher body mass, and they did not show a higher localsurvival rate than their half siblings. Hence, there was noevidence of any association between extrapair paternity andmale phenotypic or genotypic quality. Extrapair offspring wererandomly distributed among broods, with the only exceptionsof one blue tit and two great tit broods in which all young(six to nine) were sired by an extrapair male. This patternis best explained by a small proportion of males (2%–4%)being infertile and by most females performing a few extrapaircopulations as insurance against laying infertile eggs. We concludethat the results suggest a role for fertility insurance butthat alternative functional explanations to extrapair paternityin these populations cannot yet be ruled out.     

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.     

Parental investment in an anadromous population of threespine sticklebacks: An experimental study

Summary Two previously published field studies of threespine sticklebacks conducted to test predictions of parental investment (PI) theory yielded different conclusions about how males invest in their young. Males of a freshwater population invested more in older/larger broods whereas environmental factors played no role in PI decisions. In contrast, males of an anadromous population adjusted levels of PI in response to environmental factors rather than brood characteristics. The current laboratory study attempts to determine possible reasons for the discrepancy between these two studies. We addressed the following questions. Do males invest more in larger/older broods? Do environmental factors affect levels of parental investment? Males were more aggressive (a measure of PI) in defending eggs than empty nests and free-swimming fry. However, aggression was similar for different-aged eggs and different-aged fry. Moreover, when we manipulated brood sizes (fry), males did not change their level of investment. Males increased their level of aggressive defence in response to a rise in water level, indicating that they can adjust their level of investment in response to changes in environmental conditions that affect brood survival.     

Ecological opportunities and individual condition as predictors of extra‐pair paternity in a south‐temperate swallow (Tachycineta leucorrhoa)

Ecological and physiological factors such as breeding density, breeding synchrony, and adult body condition can all affect extra‐pair mating behavior, but the relative importance of these factors may vary among species. White‐rumped Swallows (Tachycineta leucorrhoa) nesting in Buenos Aires Province, Argentina, exhibit high rates of extra‐pair paternity, with 77% of nests having extra‐pair young. Our objective was to determine the extent to which extra‐pair paternity in this species is explained by breeding synchrony, breeding density, and adult body condition. Our study of a population of White‐rumped Swallows breeding in nest boxes was conducted during two consecutive breeding seasons (September – early January 2006–2008). We found that neither breeding synchrony nor density of neighbors predicted levels of extra‐pair paternity in our study population. Leaner females were more likely to engage in extra‐pair behavior and fledged more nestlings, but did not differ in structural size from females that did not engage in extra‐pair behavior, suggesting that female mass is an important predictor of mating decisions and fitness for these aerial insectivores. Male body condition was not related to male extra‐pair behavior. The mass of female White‐rumped Swallows may affect their flying ability such that, during their fertile period, they are exposed to more potential extra‐pair mates during longer foraging flights. Being lighter may also improve the ability of females to provision nestlings later in the breeding cycle.