Behavioural responses to ectoparasites in pied flycatchers Ficedula hypoleuca: an experimental study

Nests of cavity‐nesting birds usually harbor some species of haematophagous ectoparasites that feed on the incubating adults and nestlings. Given the negative impact of ectoparasites on nestlings there will be selection on hosts to reduce parasite infestations through behavioural means. We have experimentally reduced the abundance of all ectoparasites in nests of pied flycatchers Ficedula hypoleuca to explore both whether there are changes in the frequency and duration of putative anti‐parasite behaviours by tending adults, as well as whether such anti‐parasite behaviours are able to compensate for the deleterious effects that parasites may have on nestlings. Heat treatment of nests substantially decreased the density of ectoparasites, and thereby positively affected nestling growth. The frequency and intensity of female grooming and nest sanitation behaviours during the incubation and nestling periods decreased as a consequence of the experimental reduction of ectoparasite infestation. Although nestlings begged more intensely in infested nests, the experiment had no significant effect on parental provisioning effort. Reduction of parasites resulted in larger nestlings shortly before fledging and increased fledging success. This study shows a clear effect of a complete natural nest ectoparasite fauna on parental behaviour at the nest and nestling growth in a cavity‐nesting bird. Although ectoparasites induce anti‐parasite behaviours in females, these behaviours are not able to fully remove parasite's deleterious effects on nestling growth and survival.     

A review of available methods and description of a new method for eliminating ectoparasites from bird nests

Bird nests offer an ideal situation to manipulate ectoparasites and study how they impact hosts. Several methods are available to eliminate parasites from nests and each has its own suite of advantages and disadvantages. For example, recent toxicity research has revealed that some commonly used insecticides may not be suitable for use in experiments with nestlings. This highlights the need for investigators to control for the effects of methods used to eliminate nest parasites within experimental designs. Methods that can be used across treatment groups are also often needed to study the effects of variation in parasite intensity. To aid investigators in deciding which method(s) to use, we provide a comprehensive review of available methods for eliminating nest ectoparasites and also describe a new heat gun method. We tested the effectiveness of the heat‐gun method with nests of Barn Swallows (Hirundo rustica) to which 100 nest mites were added and then quantified the number of surviving mites and other naturally occurring arthropods. We found that fully heated nests had significantly fewer mites and other arthropods than partially heated or control nests. Use of the heat gun had no negative effects on nestling growth or mortality rates. In studies of avian nest ectoparasites, investigators need to consider methods that can be used across treatment groups to ensure that unaccounted for toxicity effects are not influencing results and leading to underestimation of the often subtle effects of ectoparasites on birds.     

Nest‐dwelling ectoparasites influence the start and duration of the first pre‐basic moult in the European starling Sturnus vulgaris

Nest‐dwelling ectoparasites represent an early stressor for birds as they impair the development of nestlings, which can adaptively respond by adjusting their growth rate to current conditions. While nest ectoparasites have long‐term effects on nesting adults, no study has examined if they also have an impact on the moult patterns of juveniles. Herein, we investigated whether the presence of ectoparasites in the nest influences the start and duration of the first pre‐basic moult in the European starling. To do so, we experimentally removed nest‐dwelling ectoparasites from a group of nests and used another group of unmanipulated (i.e. naturally infested) nests as the control. The moult began at an earlier age and lasted longer in birds from the ectoparasite‐free nests compared to their control counterparts. The timing of the moult was also affected by the hatching date (i.e. birds that fledged later had shorter moults) and the brood size (i.e. birds in larger broods started their moult at an older age). We also found evidence that the removal of nest ectoparasites influenced the condition of individuals during the course of the moult. In the control birds, we observed a decrease in hematocrit levels, but these were unaltered in the birds fledged from the ectoparasite‐free nests. Our study shows that nest‐dwelling ectoparasites adversely affected the timing of the moult and the individual condition of juvenile starlings, with possible major consequences for their subsequent life‐history events.     

Physiological and haematological consequences of a novel parasite on the red-rumped swallow Hirundo daurica

Parasite virulence has been hypothesised to increase with the degree of host sociality because highly social hosts have a greater probability of encountering horizontal transmission of parasites and experiencing infections with multiple strains of the same parasites than do solitary hosts. As compared with the defences of closely related social host species, we predicted that solitary hosts should have relatively weak defences against parasites, thus being relatively more affected when parasitised by a novel parasite. We tested this prediction by either experimentally infesting 12 nests of the solitarily nesting red-rumped swallow Hirundo daurica with 50 individuals of the generalist martin bug Oeciacus hirundinis or by fumigation of nine nests. Nestlings 13 days old from the parasite addition group experienced increased mortality, attained lower body mass and tended to have shorter tarsi compared to nestlings from fumigated nests. Surprisingly, nestlings from the parasite addition group had higher packed cell volume (cellular fraction of blood) and lower levels of heat shock proteins (HSP60) than nestlings from the fumigation group. A measure of immunocompetence was not significantly affected by treatment, but its magnitude was positively related to packed cell volume and negatively related to level of HSP60. Solitary hosts like the red-rumped swallow have weak immune responses and low levels of heat shock proteins when infested with ectoparasites while highly social hosts have strong immune responses and high levels of heat shock proteins when infested. These findings partially support the hypothesis that potential host species with weak defences are more susceptible to infection and the deleterious effects of evolving parasites than potential hosts with strong defences.     

Green plants in starling nests: effects on nestlings

European starlings, Sturnus vulgaris, intermingle fresh herbs, especially species rich in volatile compounds, with their otherwise dry nest material. In this field study we investigated whether these herbs reduce ectoparasites and thereby protect nestlings (the nest protection hypothesis). We also considered whether volatile compounds in herbs improve the condition of nestlings (the drug hypothesis). As measures of condition we used body mass, haematocrit levels and immunological parameters. We replaced 148 natural starling nests with artificial ones: half contained herbs and half (controls) contained grass. The ectoparasite loads (mites, lice, fleas) in herb and control nests were indistinguishable. However, nestlings in herb nests weighed more and had higher haematocrit levels at fledging than nestlings in control nests. Fledging success was similar in herb and control nests, but more yearlings from herb nests were identified in the colony the year after hatching. The response of the immune system when challenged with phytohaemagglutinin did not differ in nestlings from herb and control nests. Nestlings from herb nests had more basophils and fewer lymphocytes in their blood than those from control nests, while the eosinophil and heterophil counts did not differ. We conclude that herbs do not reduce the number of ectoparasites, but they improve the condition of nestlings, perhaps by stimulating elements of the immune system that help them to cope better with the harmful activities of ectoparasites. Copyright 2000 The Association for the Study of Animal Behaviour.     

Nest excavation does not reduce harmful effects of ectoparasitism: an experiment with a woodpecker, the northern flicker Colaptes auratus

It has been hypothesized that it is adaptive for birds to build new nests annually in order to avoid the accumulation of ectoparasites. Previous studies on costs of ectoparasitism have focused on cavity nesters in nestboxes while largely ignoring reproductive consequences in natural tree cavity nests, the context where nest selection strategies presumably evolved. To see whether ectoparasitism could be a driving selective force in the evolution of nest excavation in a woodpecker, I experimentally fumigated a subset of freshly excavated cavities and a subset of reused cavities of the northern flicker Colaptes auratus and compared reproductive performance with a set of control nests. The main ectoparasite of nestlings, a blood-sucking fly Carnus hemapterus , may have appeared one or two days earlier in reused nests but there was no difference between fresh and reused nests in intensities of flies one week post-hatching. Prevalence of parasitism reached 100% in both reused and freshly-excavated control nests in the second week. Nestlings from control nests had lower body mass residuals than those from fumigated nests after 15 d and fledged at a lower weight, suggesting that ectoparasitism by C. hemapterus was costly. However, fresh nest construction was no benefit, likely because the high dispersal ability of the ectoparasite meant all nests were colonized rapidly. Parents did not adjust provisioning effort according to parasitism as delivery rates did not differ between control and fumigated nests but delivery rates increased with brood size.     

An experimental test of predator–parasite interaction in a passerine bird

Experimental studies incorporating multiple trophic levels are scarce but of increasing interest for understanding ecological communities. Here we investigated interactive effects of perceived predation risk and parasite pressure on life‐history traits in a hole‐nesting bird, and the effects of predation risk on parasite success. In a 3 × 2 experimental design we increased perceived predation risk for breeding great tits Parus major via simulations of either nest‐predators (woodpeckers) or post‐fledging predators (sparrowhawks) close to nests, and used a non‐predatory species (song thrush) as a control. Concurrently, half of the nests in each treatment were either infested with ectoparasites, or kept parasite‐free. Regarding the predation risk – parasite interaction, exposure to nest‐predators tended to lower wing and sternum growth rates of nestlings in the absence, but not the presence, of parasites. In the presence of parasites, exposure to a post‐fledging, but not to a nest‐predator, led to significantly reduced wing growth. Mass and tarsus length were not affected by predator exposure, but ectoparasites had slight positive effects on mass gain. In the last third of the nestling period, overall nestling size was significantly smaller when exposed to a post‐fledging predator than to a nest‐predator, but neither differed from the control. Parental feeding rates were not affected by the treatments, but parents became less selective towards food items under either predation risk. Hen‐flea population sizes (adult or larvae) in nests were not affected by predation risk treatment of hosts. In summary, we found some evidence for an interactive effect of predation risk and parasite pressure on nestling growth. The complexity of the interaction, combined with certain inconsistencies of the effects and potential statistical artifacts, prevent however a straightforward interpretation of the results. The insights from the study are useful for designing additional experiments to further investigate the complexity of predator–parasite interactions in wild populations.     

Adaptive host-abandonment of ectoparasites before fledging? Within-brood distribution of nest mites in house sparrow broods

We studied the within-brood distribution of a haematophagous mite Pellonyssus reedi living on nestling house sparrows (Passer domesticus) near the time of fledging. We measured the natural level of infestation of individual nestlings, and determined the feeding efficiency of mites, by scoring their feeding status. Within-brood distribution of mite loads was unrelated to nestling body mass, tarsus length, or immunocompetence. These results did not support parasite preference for large or susceptible hosts. Mite feeding-efficiency was also unrelated to these nestling characteristics, confirming that large nestlings or nestlings with less-developed immunocompetence did not provide superior feeding conditions for mites. Therefore, our results do not support the hypothesis that within-brood distribution of avian ectoparasites is explained by the parasites' preferences for characteristics, such as large body size or low immunocompetence, that make nestlings suitable hosts. On the other hand, we found that mite loads were negatively correlated with nestling age and feather length, suggesting that nestlings closer to fledging harbored fewer mites then their less-developed nestmates. Furthermore, feather length had a stronger relationship with parasite distribution than did nestling age. We presume, therefore, that feather characteristics, i.e., length, may serve as a signal for mites to perceive the ready-to-fledge state of nestlings, inducing abandonment behavior. These results support another, largely neglected hypothesis, i.e., that the avoidance or abandonment of those nestlings that are close to fledging may also explain the parasites' distribution in a brood. This hypothesis is based on the argument that many nest-dwelling ectoparasites breed in the nest material and emerge only periodically to feed on nestlings. In such parasites, the ability to recognize and avoid mature fledglings can be adaptive because this may help the parasites to avoid their removal from the nest so they can continue to reproduce by feeding on unfledged chicks of the current or later broods. Our results suggest that adaptive host-abandonment by nest-dwelling ectoparasites can influence within-brood parasite distributions around the time of fledging.     

Palatability of passerines to parasites: within-brood variation in nestling responses to experimental parasite removal and carotenoid supplementation

Asynchronous hatching of eggs in avian clutches produces a size hierarchy among nestlings that may lead to variation within broods in resistance to pathogens or parasites. In this study, we tested several predictions regarding variation in immunocompetence and distribution of parasites within avian broods by combining parasite removal and carotenoid supplementation treatments in nests of mountain bluebirds Sialia currucoides . Last-hatched nestlings were less likely to invest carotenoids in an induced cell-mediated immune response, suggesting they may be more susceptible to parasites; however, parasite removal disproportionately benefited middle-ranked nestlings. This supports the hypothesis that some avian ectoparasites balance host resistance against nutritional benefits by preferentially parasitizing nestlings of intermediate quality and immunocompetence. We found no evidence that males positioned last in the hatching sequence were differentially affected by ectoparasites, and, contrary to some previous studies in other passerines, last-hatched nestlings in asynchronously hatching broods were not less immunocompetent than their nest mates. In fact, junior nestlings exhibited weaker immune responses than their siblings in more synchronously hatching broods, and we suggest this may reflect environment-dependent maternal effects that warrant further investigation. Overall, our results highlight the importance of understanding the feeding and host selection behaviour of ectoparasites, as well as the fitness consequences thereof, since many predictions related to within-brood distribution of parasites require that parasites are able to discern the relative quality of available hosts.     

Determinants of abundance and effects of blood-sucking flying insects in the nest of a hole-nesting bird

Compared to non-flying nest-dwelling ectoparasites, the biology of most species of flying ectoparasites and its potential impact on avian hosts is poorly known and rarely, if ever, reported. In this study we explore for the first time the factors that may affect biting midge (Diptera: Ceratopogonidae) and black fly (Diptera: Simuliidae) abundances in the nest cavity of a bird, the hole-nesting blue tit Cyanistes caeruleus, and report their effects on adults and nestlings during reproduction. The abundance of biting midges was positively associated with nest mass, parental provisioning effort and abundance of blowflies and black flies, while negatively associated with nestling condition. Furthermore, a medication treatment to reduce blood parasitaemias in adult birds revealed that biting midges were more abundant in nests of females whose blood parasitaemias were experimentally reduced. This finding would be in accordance with these insect vectors attacking preferentially uninfected or less infected hosts to increase their own survival. The abundance of black flies in the population was lower than that of biting midges and increased in nests with later hatching dates. No significant effect of black fly abundance on adult or nestling condition was detected. Blood-sucking flying insects may impose specific, particular selection pressures on their hosts and more research is needed to better understand these host–parasite associations.     

The price of insulation: costs and benefits of feather delivery to nests for male tree swallows Tachycineta bicolor

Many species of birds line their nests with feathers, and it has been hypothesized that this functions to provide a thermally stable microenvironment for the development of eggs and nestlings. Feathers in the nest may also function as a mechanism for parasite control, providing a physical barrier that protects nestlings from ectoparasites. We tested these hypotheses by performing a feather removal and addition experiment in tree swallows Tachycineta bicolor, a species well‐known for lining their nests with feathers. While we found no evidence that quantity of feathers in nests influenced the ability of females to produce and incubate eggs, offspring in well‐feathered nests had longer flight feathers and were structurally larger just prior to fledging that those in nests with fewer feathers. Furthermore, we also demonstrated a positive correlation between feathers and the abundance of larval blow flies Protocalliphora spp. in nests, a result opposite to that predicted by the anti‐parasite hypothesis. While our study provides strong support for the insulation hypothesis, we also discuss the possibility that devoting time to feather gathering may result in males losing paternity in their nests, although manipulative studies will be necessary to fully evaluate this idea.     

Nestling sex predicts susceptibility to parasitism and influences parasite population size within avian broods

Vertebrate hosts differ in their level of parasite susceptibility and infestation. In avian broods, variation in susceptibility of nestlings to ectoparasites may be associated with non‐uniform distributions of parasites among brood mates, with parasites concentrating feeding on the most vulnerable hosts. The presence of a highly susceptible nestling in a brood can benefit the remaining young by reducing the parasite pressure they experience; however, from a parasite’s perspective, broods with fewer susceptible hosts may provide effectively fewer resources than broods of the same size containing a greater abundance of susceptible hosts, and this could limit the number of parasites that a host brood can sustain. To test whether variation in number of susceptible hosts affects the number of parasites in bird nests, we first examined the role of host sex and induced immunity (via methionine supplementation) on susceptibility of mountain bluebirds Sialia currucoides to parasitism by blow flies Protocalliphora spp. We then assessed the effect of variation in number of susceptible hosts on the number of parasites inhabiting the nest. Only females showed a benefit of methionine supplementation, gaining mass more rapidly following supplementation compared to males. This suggests that females are more susceptible to parasites in this system; this was further supported by parasite feeding trials, in which parasites extracted larger blood meals from female than male hosts. Finally, the abundance of parasites in nests was predicted by brood sex ratio: broods containing more female young harboured more parasites. Hence, within‐brood variation in host susceptibility to parasites can not only influence the costs of parasitism for individual nestlings, but may also have consequences for the size of parasite populations within nests. If patterns of maternal investment affect the abundance of nest‐dwelling parasites, these interactions may be important for understanding fitness consequences of maternal resource allocation in many vertebrate hosts.     

Induced responses of nestling great tits reduce hen flea reproduction

The dynamics of host–parasite interactions depend to a large extent on the effect of host responses on parasite fitness. Exposure to parasites may induce behavioural or physiological responses in hosts that may reduce the subsequent survival or reproductive output of the parasite. Neonate hosts may further directly obtain immunologically active substances from their mother, for instance via milk in mammals or egg yolk in birds. However, the relative importance of maternally‐derived and self‐generated responses in inducing parasite resistance is poorly understood, especially in free‐living vertebrates. Here we investigate the complementary effect of experimentally induced maternal and neonate responses in great tit (Parus major) hosts on the reproductive success of their common ectoparasite, the hen flea (Ceratophyllus gallinae). In the laboratory we measured the number of eggs and larvae produced by individual flea females collected from host nests. In addition, the total number of larvae produced by an experimentally set number of flea females in the host's nestbox was assessed under field conditions. There was no indication of maternally‐transferred parasite resistance, since exposing the mother to fleas during the laying period did not affect the reproductive rate of fleas exploiting her offspring early or late in the nestling cycle. Independent of the maternal treatment, exposure of neonates to fleas early in the nestling period reduced the reproductive output of fleas late in the nestling cycle. The effect of the induced nestling response was seasonal, reducing flea reproduction in nests of early‐breeding hosts but not in nests of late‐breeding ones. Larvae production in the nestbox and in the laboratory was positively correlated, but under natural conditions the neonate response did not affect the size of the flea larvae population. Our results indicate induced responses as a means by which neonate avian hosts resist ectoparasites. Other factors, such as the environmental temperature and density‐dependent larval competition, may be more important in determining the size of the future parasite populations.     

Ectoparasitism and the role of green nesting material in the European starling

Summary The use of green nesting material is widespred among birds. Recent evidence suggests that birds use secondary chemicals contained in green plants to control ectoparasites. We manipulated green nesting material and ectoparasites of European starlings (Sturnus vulgaris) to test two hypotheses: (1) ectoparasites adversely affect prefledging survival and morphometrics or postfledging survival, and (2) green nesting material ameliorates the effects of ectoparasites. We recorded fat score, numbers of scabs, tarsal length, body mass, and hematocrit level on each nestling 17 days after hatching. We also fitted each nestling with unique patagial tags and resighted the starlings for 6–8 weeks after fledging to estimate survival and sighting rates. Nests devoid of green nesting material and dusted with the insecticide, carbaryl, had fewer high ectoparasite infestations, and nestlings had significantly lower scab scores, and significantly higher body masses than nestlings in undusted boxes. However, there was no difference in postfledging survival between birds from carbaryl-treated and undusted nests. There also was no difference in prefledging survival and morphometrics or postfledging survival between nestlings from boxes with and without green nesting material. These results do not support the hypothesis that starlings use green nesting material to control nest ectoparasites. We suggest an alternative hypothesis; green nesting material is used for mate selection or pairbonding in the starling.     

The process of fledging in the Mountain Bluebird

Fledging is a critical event in the avian breeding cycle, but remains unstudied in almost all species. As a result, little is known about factors that cause nestlings to leave nests. We documented fledging behavior in a box‐nesting population of Mountain Bluebirds (Sialia currucoides) using radio‐frequency identification. We attached a passive integrated transponder (PIT tag) to the leg of each nestling in 40 nests. An antenna checked for the presence of a transponder signal (i.e., a nestling) at nest‐box entrances every 2 s. The time of last detection of a nestling was taken as the time that nestling fledged. We found that fledging began when the oldest nestlings were 15–22 d old. Broods that were ahead in development, as measured by primary feather length, fledged at relatively younger ages. All nestlings fledged on the same day at 33 nests (83%) and over 2 d at remaining nests. When all nestlings fledged on the same day, fledging usually began in the morning and median time between the first and last fledging was 55 min (range = 2.3 min–10.6 h). When young fledged over 2 d, fledging always began >8 h after sunrise and usually just one nestling fledged the first day, suggesting that this fledging may have been accidental. Clutches in our population often hatch asynchronously, which sets up a hierarchy within broods in developmental state, size, and competitive ability. In such situations, fledging may be initiated by one of the most‐developed and hence most‐competitive nestlings in a brood, presumably when it reaches a certain threshold state of development. Alternatively, fledging may begin when a less‐developed, less‐competitive, and probably hungrier nestling leaves the nest, presumably to gain better access to food. We used the proportion of time that a nestling was able to occupy the nest‐box entrance late in the nestling stage, waiting to intercept parents with food, as an index of nestling competitive ability. Assuming that the number of nest entrance detections reliably indicates nestling competitive ability, we found that the most‐competitive nestling fledged first at over half of all nests, supporting the notion that fledging usually begins when oldest nestlings reach a threshold state of development.     

Maternal effects reduce oxidative stress in female nestlings under high parasite load

Mothers can adjust the phenotype of their offspring to the local environment through a modification of their egg investment and/or nestling provisioning. However, offspring health may be severely impaired if the conditions experienced by nestlings do not match with those anticipated by the mother. If maternal effects differentially affect the sexes or if one sex is more strongly affected by an environmental stressor, fitness benefits may also differ between male and female offspring. Here, we study maternal effects in male and female great tit Parus major nestlings by means of an ectoparasite treatment before egg‐laying combined with a partial cross‐foster experiment between broods of infested and uninfested nests. Nestlings that were raised in their own nest experienced the same conditions before and after cross‐fostering (either in parasite infested or uninfested nests), while cross‐fostered ones experienced different conditions (either changing from infested to uninfested or the other way around). We measured effects on nestling plasma levels of oxidative stress [reactive oxygen metabolites (ROMs) and total antioxidant capacity (OXY)], body condition (body size and mass) and post‐fledging survival. Daughters, but not sons, from matching conditions showed the lowest ROM and high OXY levels when exposed to parasites, while there was no effect of parasite exposure in any of both sexes in case of a mismatch. In contrast, body condition and post‐fledging survival were not (or only slightly) affected by any of the experimental treatments. Results of this study show that maternal effects can affect oxidative stress levels of nestlings in a sex‐specific way and that the outcome depends on the exposure to environmental stressors, such as parasites.     

Females compensate for moult‐associated male nest desertion in Hooded Warblers

Uniparental offspring desertion occurs in a wide variety of avian taxa and usually reflects sexual conflict over parental care. In many species, desertion yields immediate reproductive benefits for deserters if they can re‐mate and breed again during the same nesting season; in such cases desertion may be selectively advantageous even if it significantly reduces the fitness of the current brood. However, in many other species, parents desert late‐season offspring when opportunities to re‐nest are absent. In these cases, any reproductive benefits of desertion are delayed, and desertion is unlikely to be advantageous unless the deserted parent can compensate for the loss of its partner and minimize costs to the current brood. We tested this parental compensation hypothesis in Hooded Warblers Setophaga citrina, a species in which males regularly desert late‐season nestlings and fledglings during moult. Females from deserted nests effectively doubled their provisioning efforts, and nestlings from deserted nests received just as much food, gained mass at the same rate, and were no more likely to die from either complete nest predation or brood reduction as young from biparental nests. The female provisioning response, however, was significantly related to nestling age; females undercompensated for male desertion when the nestlings were young, but overcompensated as nestlings approached fledging age, probably because of time constraints that brooding imposed on females with young nestlings. Overall, our results indicate that female Hooded Warblers completely compensate for male moult‐associated nest desertion, and that deserting males pay no reproductive cost for desertion, at least up to the point of fledging. Along with other studies, our findings support the general conclusion that late‐season offspring desertion is likely to evolve only when parental compensation by the deserted partner can minimize costs to the current brood.     

The Process and Causes of Fledging in a Cavity-Nesting Passerine Bird, the House Wren (Troglodytes aedon)

Little is known about the process or causes of fledging or nest‐leaving in passerine birds because researchers can rarely predict when fledging will occur in a given nest. We used continuous videotaping of nests to both document the process of fledging in the house wren, Troglodytes aedon, a small, cavity‐nesting songbird, and test hypotheses as to what might cause fledging to begin. Fledging began any time from 14 to 19 d after hatching commenced. Slower‐developing broods fledged later than faster‐developing broods. Fledging typically began within 5 h of sunrise and over 80% of all nestlings fledged before noon. All nestlings fledged on the same day at 65% of nests and over two consecutive days in most other nests. We found no evidence that fledging was triggered by changes in parental behaviour. Parental rate of food delivery to nestlings did not decline during a 3‐h period leading up to the first fledging, nor was the rate of feeding just prior to the first fledging lower than the rate at the same time the day before. Moreover, parents did not slow the rate of food delivery to nests after part of the brood had fledged. Hatching is asynchronous in our study population which creates a marked age/size hierarchy within broods. At most nests, the first nestling to fledge was the most well‐developed nestling in the brood or nearly so (as measured by feather length). This suggests that fledging typically begins when the most well‐developed nestlings in the brood reach some threshold size. However, at about one‐fifth of nests, the first nestling to fledge was only moderate in size. At these nests, severe competition for food may have caused smaller, less competitive nestlings to fledge first to increase their access to food. We found no strong support for the suggestion that the oldest nestlings delay fledging until their least‐developed nestmate reaches some minimum size, although further experimental work on this question is warranted.     

Behavior of adult and young grassland songbirds at fledging

The behavior of adults and young at the time of fledging is one of the least understood aspects of the breeding ecology of birds. Current hypotheses propose that fledging occurs either as a result of parent‐offspring conflict or nestling choice. We used video recordings to monitor the behavior of nestling and adult grassland songbirds at the time of fledging. We observed 525 nestlings from 166 nests of 15 bird species nesting in grasslands of Alberta, Canada, and Wisconsin, USA. Overall, 78% of nestlings used terrestrial locomotion for fledging and 22% used wing‐assisted locomotion. Species varied in propensity for using wing‐assisted locomotion when fledging, with nestling Grasshopper Sparrows (Ammodramus savannarum) and Henslow's Sparrows (Centronyx henslowii) often doing so (47% of fledgings) and nestling Song Sparrows (Melospiza melodia), Common Yellowthroats (Geothlypis trichas), and Chestnut‐collared Longspurs (Calcarius ornatus) rarely doing so (3.5% of fledgings). For 390 fledging events at 127 nests, camera placement allowed adults near nests to be observed. Of these, most young fledged (81.5%) when no adult was present at nests. Of 72 fledging events that occurred when an adult was either at or approaching a nest, 49 (68.1%) involved feeding. Of those 49 fledgings, 30 (62.1%) occurred when one or more nestlings jumped or ran from nests to be fed as an adult approached nests. The low probability of nestlings fledging while an adult was at nests, and the tendency of young to jump or run from nests when adults did approach nests with food minimize opportunities for parents to withhold food to motivate nestlings to fledge. These results suggest that the nestling choice hypothesis best explains fledging by nestlings of ground‐nesting grassland songbirds, and fledging results in families shifting from being place‐based to being mobile and spatially dispersed.     

Do parasites and antioxidant availability affect begging behaviour,growth rate and resistance to oxidative stress?

Early‐life trade‐offs faced by developing offspring can have long‐term consequences for their future fitness. Young offspring use begging displays to solicit resources from their parents and have been selected to grow fast to maximize survival. However, growth and begging behaviour are generally traded off against self‐maintenance. Oxidative stress, a physiological mediator of life‐history trade‐offs, may play a major role in this trade‐off by constraining, or being costly to, growth and begging behaviour. Yet, despite implications for the evolution of life‐history strategies and parent–offspring conflicts, the interplay between growth, begging behaviour and resistance to oxidative stress remains to be investigated. We experimentally challenged wild great tit (Parus major) offspring by infesting nests with a common ectoparasite, the hen flea (Ceratophyllus gallinae), and simultaneously tested for compensating effects of increased vitamin E availability, a common dietary antioxidant. We further quantified the experimental treatment effects on offspring growth, begging intensity and oxidative stress. Flea‐infested nestlings of both sexes showed reduced body mass during the first half of the nestling phase, but this effect vanished short before fledging. Begging intensity and oxidative stress of both sexes were unaffected by both experimental treatments. Feeding rates were not affected by the experimental treatments, but parents of flea‐infested nests fed nestlings with a higher proportion of caterpillars, the main source of antioxidants. Additionally, female nestlings begged significantly less than males in control nests, whereas both sexes begged at similar rates in vitamin E‐supplemented nests. Our study shows that a parasite exposure does not necessarily affect oxidative stress levels or begging intensity, but suggests that parents can compensate for negative effects of parasitism by modifying food composition. Furthermore, our results indicate that the begging capacity of the less competitive sex is constrained by antioxidant availability.