Responses of naive yellow warblers to a novel nest predator

Naive parental yellow warblers, Dendroica petechia, were tested with a mounted eastern grey squirrel, Sciurus carolinensis, a novel predator on the study site, during the nest-building, egg-laying, incubation and nestling stages of the nesting cycle. Testing parents only once avoided the possibility that the nest defence behaviour of the parents was modified by reinforcement and loss of fear. In 96% of 80 trials, the female parent responded first to the model. Males rarely showed nest defence behaviour. Female nest defence as measured by defensive vocalizations (i.e., ‘chipping’), closest and modal distance of approach to the model, distraction displays, strikes, and close passes or hovers, did not increase significantly over the breeding season. ‘Chipping’ frequency by both sexes tended to increase after the incubation period but not significantly so. Distraction displays increased significantly only between nest-building and nestling stages. Age, clutch or brood size, and nest success were not correlated with the intensity of nest defence. Females defending exposed nests gave more distraction displays than those defending cryptic nests.     

Habitat-specific clutch size and cost of incubation in eiders reconsidered

The energetic incubation constraint hypothesis (EICH) for clutch size states that birds breeding in poor habitat may free up resources for future reproduction by laying a smaller clutch. The eider (Somateria mollissima) is considered a candidate for supporting this hypothesis. Clutch size is smaller in exposed nests, presumably because of faster heat loss and higher incubation cost, and, hence, smaller optimal clutch size. However, an alternative explanation is partial predation: the first egg(s) are left unattended and vulnerable to predation, which may disproportionately affect exposed nests, so clutch size may be underestimated. We experimentally investigated whether predation on first-laid eggs in eiders depends on nest cover. We then re-evaluated how nesting habitat affects clutch size and incubation costs based on long-term data, accounting for confounding effects between habitat and individual quality. We also experimentally assessed adult survival costs of nesting in sheltered nests. The risk of egg predation in experimental nests decreased with cover. Confounding between individual and habitat quality is unlikely, as clutch size was also smaller in open nests within individuals, and early and late breeders had similar nest cover characteristics. A trade-off between clutch and female safety may explain nest cover variation, as the risk of female capture by us, mimicking predation on adults, increased with nest cover. Nest habitat had no effect on female hatching weight or weight loss, while lower temperature during incubation had an unanticipated positive relationship with hatching weight. There were no indications of elevated costs of incubating larger clutches, while clutch size and colony size were positively correlated, a pattern not predicted by the ‘energetic incubation constraint’ hypothesis. Differential partial clutch predation thus offers the more parsimonious explanation for clutch size variation among habitats in eiders, highlighting the need for caution when analysing fecundity and associated life-history parameters when habitat-specific rates of clutch predation occur.     

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.     

Effects of biotic and abiotic factors on the oxygen content of green sea turtle nests during embryogenesis

Several biotic and abiotic factors can influence nest oxygen content during embryogenesis. Several of these factors were determined during each developmental stage of green sea turtle embryos on Wan-an Island, Penghu Archipelago, Taiwan. We examined oxygen content in 7 nests in 2007 and 11 in 2008. Oxygen in the adjacent sand, total and viable clutch sizes, air, sand and nest temperatures, and sand characters of each nest were also determined. Oxygen content was lower in late stages than in the early and middle stages. It was also lower in the middle layer than in the upper and bottom layers. Nest temperature showed opposite trends, reaching its maximum value in late stages of development. Nest oxygen content was influenced by fraction of viable eggs, total clutch sizes, sand temperatures, maximum nest temperature and maximum change in the nest temperature during incubation. Clutch size during embryogenesis was the most influential factor overall. However, the major influential factors were different for different developmental stages. In the first half of the incubation, the development rate was low, and the change in the nest oxygen content was influenced mainly by the clutch size. During the second half, the rapid embryonic development rate became the dominant factor, and hatchling activities caused even greater oxygen consumption during the last stage of development.     

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.     

Parental Investment Theory and Nest Defence by Imperial Shags: Effects of Offspring Number,Offspring Age,Laying Date and Parent Sex

Nest defence is a common form of parental care employed by birds to improve the survival of their offspring. Theory predicts that parents should adjust their nest defence according to the value of the brood at stake, defending more intensively broods with high survival and reproductive prospects. We evaluated the influence of offspring number, offspring age, laying date and parent sex on nest‐defence intensity (NDI) of the Imperial Shag Phalacrocorax atriceps, a sexually dimorphic seabird with seasonal decline in offspring survival and very limited renesting potential. We also evaluated whether NDI was correlated within pairs and whether NDI of both members of the pair was correlated with incubation and breeding success. To elicit defensive behaviour, we simulated predation attempts using a Kelp Gull Larus dominicanus model. As predicted by theory, NDI was positively correlated with the number of offspring in the nest and offspring age. NDI during chick rearing was higher than that at early and late incubation, while no differences were found between incubation stages. Contrary to our prediction, we did not find differences in NDI according to laying date. NDI for males was higher than females, while NDI was also positively correlated within pairs. NDI was not statistically related to incubation or breeding success. These results suggest that other factors, such as laying date or parental quality and age, play a much larger role in determining the outcome and productivity of a nesting attempt. Our results provide partial support for parental investment theory; while parental defence increased with brood value according to offspring number and age, parental defence was not related to laying date, a factor strongly affecting offspring survival and recruitment probabilities in this species.     

Effectiveness of nest defence in the Acadian Flycatcher Empidonax virescens

We used presentations of models to determine the effectiveness of nest defence in the Acadian Flycatcher Empidonax virescens against a nest predator (Blue Jay Cyanocitta cristata ) and a brood parasite (Brown-headed Cowbird Molothrus ater ). Principal components analysis (PCA) of four component variables of nest defence (call rate, swoop rate, closest approach and number of adults) generated a measure of overall nest defence (aggression). We determined effectiveness of defence by looking for correlations between measures of defence and measures of nest success (nest predation and brood parasitism). We also determined whether nest defence increased with clutch size, nestling age and time in the breeding season. Defence against model Brown-headed Cowbirds did not correlate with levels of parasitism, clutch size, age of young or time of breeding. There was, however, a strong, but insignificant, trend for nests with high levels of all measures of defence to suffer less from brood parasitism. Aggression, vocalization rate, closest approach and number of adults defending against models of predatory Blue Jays correlated positively with nesting success during the egg stage but not the nestling stage of the nesting cycle. Aggression, vocalization rate, closest approach correlated with clutch size and age of the brood. These results suggest that nest defence can effectively deter nest predators, but may be less effective against brood parasites. Different behavioural components of nest defence may work at different stages of the nest cycle and against different nest predators. The components of nest defence that correlated with nest success also correlated with clutch value, a result consistent with hypotheses on the evolution of nest defence.     

Nest desertion: a trade-off between current and future reproduction

Life history theory predicts that parents should desert a reproductive attempt if the costs of rearing this brood exceed the expected benefits. Thus, if the value of the current breeding attempt is reduced, for example through an unexpected reduction in size, parents are expected to reconsider whether it is worth continuing investing in their brood. With regard to nest desertion behaviour two predictions can be made: individuals are (1) more likely to desert if the reduction in clutch size is large and (2) less likely to desert if the reduction is at a late stage of breeding. We investigated the threshold at which nest desertion takes place by experimentally reducing great tit, Parus major, clutches to different sizes and at different stages of the incubation period. The results were in accordance with the predictions: clutch desertion rates were negatively related to the number of eggs that remained in the nest, and nest desertion was less likely nearer the end of the incubation period. In addition, we estimated the fitness consequences of nest desertion behaviour. For this purpose we made one group of birds desert in favour of a replacement clutch and another group rear a reduced brood. The latter were more likely to produce a second clutch after the first-brood fledglings had left the nest. As a consequence, the number of fledglings produced over the entire breeding season did not differ between the two experimental groups. We also counted the number of recruits and breeding adults in the following breeding season and found that the experimental groups did not differ in local recruitment and adult survival. Therefore, the results did not indicate that parents improved their fitness by deserting a reduced clutch.Copyright 2002 The Association for the Study of Animal Behaviour. Published by Elsevier Science Ltd. All rights reserved .     

Female great tits Parus major do not increase their daily energy expenditure when incubating enlarged clutches

Several studies have shown that enlargement of clutches during incubation reduces the long-term survival of parents. In line with these findings, studies on the energetic costs of nocturnal incubation show an increase in energy expenditure with clutch enlargement. Studies on daily energy expenditure during incubation (DEE_inc), however, do not consistently show such a negative effect of clutch enlargement. To determine whether differential survival results from a direct increase in energy costs or rather from costs associated with compensatory behaviour, we studied the DEE_inc (kJ day⁻¹), change in body mass and nest attendance behaviour of free-living female great tits Parus major that incubated either control or experimentally enlarged clutches. DEE_inc did not differ between the two treatment groups, but was negatively related to mean ambient temperature over the 24-h measuring period, and to the fraction of daytime females spent on the nest. Controlling for these two factors, females incubating enlarged clutches did not spend more energy per 24 h period than females incubating control clutches. Clutch enlargement also did not affect body mass of incubating females, or their nest attendance behaviour. Yet, in the enlarged group body mass change and nest attentiveness were negatively correlated, suggesting that females responded differently to the experimental treatment and thereby preventing us from finding an effect of clutch enlargement.     

Correlation between two components of parental investment: nest defence intensity and nestling provisioning effort of willow tits

Nest defence intensity and nestling provisioning effort of female willow tits (Parus montanus) were significantly correlated at the end of nestling period: well-fed young were defended most intensely. Increased effort was rewarded, since broods with the highest female per-offspring provisioning rates were the most likely to produce local recruits. This suggests that the feeding ability is an important cue for parental investment decisions, at least in a species like the willow tit which has adopted the clutch adjustment strategy. Thus, the most valuable broods would not necessarily be the largest ones, but the ones in which the original number of young could be fed most adequately. However, no associations were found between the level of parental effort and offspring weight, size or condition, nor did the broods producing recruits differ from other broods in timing of breeding or number and size of offspring. The female behaviour may suggest that they invest the most time, energy and risk in the young whose chances of joining the winter flock are the best. The first well-fed young also gain an advantage of prior residency in joining the flock. The first to join normally obtain higher social status, and hence better winter survival, than latecomers. The corresponding patterns in male parental investment behaviour were weak or absent, which suggested that the male effort was affected by the female behaviour. Males seemed to invest in nestling provisioning in such a way as to supplement the female effort. During nest defence action males also seemed to invest in protection of females against predation.     

Effects of clutch sizes and incubation stage on nest desertion in the female Common Eider Somateria mollissima nesting in the high Arctic

In bird species, one of the trade-offs between reproduction and survival appears in the parental decision to desert the nest. Nest desertion is modulated by several factors including clutch size. However, the incubation stage at which predation occurs is also an important factor. In this study, we examined whether nest desertion was linked to initial clutch size, partial clutch predation (final clutch size) and the incubation stage at which it happened in a capital breeder: the female common eider (Somateria mollissima) nesting in the high Arctic. The study was performed in Kongsfjorden in 2002 on the western coast of the Svalbard Archipelago (78°55′N, 20°07′E). We observed that nest desertion was higher when the initial clutch size was small. Also, females deserted their nests more during the first third of incubation than later. Thus, as incubation proceeded, nest desertion was less likely to occur even after egg reduction. Our results pointed out that this parental decision in female eiders seemed to depend on initial clutch size and on the date into incubation of clutch reduction. Sophie Bourgeon and Francois Criscuolo contributed equally to the work     

Body-Mass, Composition, and Survival of Nestling and Fledgling Starlings (

Earlier studies of the starling (Sturnus vulgaris) population at Belmont, Lower Hutt, New Zealand, showed that nest productivity was low compared with other populations in New Zealand and elsewhere. Therefore, we investigated possible trade-offs between offspring number and quality (as measured by body mass and composition). We also compared these measures of offspring condition with pre- and post-fledging survival. Nestling mass did not significantly differ with clutch size or brood size at any age. In starlings about to leave the nest, lean (i.e., fat-free) dry mass and water mass increased with body mass, but lipid mass increased approximately twice as much. When the effects of the other variables were controlled in a partial correlation analysis, lean dry mass, water mass, lipid mass, and mass of stomach contents were positively correlated with mass at nest-leaving; brood size was not correlated with mass at nest-leaving. Nest success was independent of clutch size and brood size, but lighter broods were more likely to fail totally than were heavier broods early in the nestling period. Nestling survival early, but not late, in the nestling period was positively correlated with nestling mass. The likelihood that a nestling raised in 1973-1979 would be recruited as a breeder was independent of its mass at brood- day 12. Thus, unlike some other passerines, larger, heavier starling nestlings did not seem to survive better than average ones. Low productivity was not accompanied by a decrease in body condition of those nestlings that survived the nestling period. Therefore, starlings at Belmont reduced offspring number rather than offspring quality when they encountered unfavourable conditions.     

Aggressiveness in king penguins in relation to reproductive status and territory location

King penguins, Aptenodytes patagonicus, vigorously defend small territories in very dense colonies. The egg-laying season lasts approximately 4 months, but only pairs that reproduce during the first half of the period succeed in fledging a chick. I examined various factors affecting aggressiveness of king penguins during the breeding season and focused on the differences between central and peripheral territories. Pairs on peripheral territories experienced twice as many encounters with avian predators as did central birds. The vast majority of peripheral birds were late breeders, indicating that reproductive success was very low among penguins defending a territory on the edge of the colony. Time invested in territory defence and rate of agonistic encounters between breeding neighbours increased from the incubation to the brooding period. Parents gave most threat displays to territorial neighbours when the chick was very young and just before crèche formation. Distance to colony edge was not related to aggressiveness in incubating birds, however, the rate of pecking and flipper blows increased from the edge to the centre during brooding. In addition, aggressiveness of breeding penguins towards travelling birds trespassing into their territory increased with distance to edge. Early breeders were not more aggressive than late breeders but the proportion of time spent in territory defence increased with the number of days a bird had spent incubating. As expected, I did not detect any sex difference in aggressive behaviour. Birds occupying territories on the beach were generally more aggressive during the incubation period than those located on the valley sides. Reproductive status (incubating versus brooding) and territory location were the main factors explaining the various levels of aggressiveness observed in breeding king penguins. Copyright 2000 The Association for the Study of Animal Behaviour.     

The feminizing effect of metabolic heating in Green Turtle (Chelonia mydas) clutches in the eastern Mediterranean

Metabolic heating has been poorly investigated in eastern Mediterranean coastline of Turkey, which host some of the most important Green Turtle (Chelonia mydas) nesting sites in the Mediterranean. We studied the effects of clutch size and embryo numbers on nest temperature and discuss the feminizing effect of metabolic heating. Two test sites were conducted in Sugözü Beaches (Turkey). Data loggers were placed in eight nests with different clutch sizes. Nest temperature was strongly correlated with embryo numbers and metabolic heating produced by embryos was calculated to be 0.019°C per late stage embryo and 0.020°C per hatchling. Metabolic heating was calculated to be 0.6°C in the middle third of the incubation period during which sex is determined. It was estimated that metabolic heating increased 10.4% of female hatchlings. The heat produced by embryos should be taken into consideration while estimating sex ratios indirectly by nest and sand temperatures. Additionally, the metabolic heating value should be known for conservation measures, such as nest relocation, dividing the nest for controlling nest temperature, especially related to climate change.     

Parental defence in Long-eared Owls Asio otus: effects of breeding stage, parent sex and human persecution

The responses of male and female Long-eared Owls to a human approaching the nest were examined. Each nest was only tested once. Nest defence increased significantly throughout the breeding season because older chicks were defended more strongly than younger chicks and eggs. No correlations were however found between defence intensity and laying date, clutch- or brood-size. These results generally do not support either the renesting-potential hypothesis or the positive reinforcement hypothesis but are in accordance with both the age-investment hypothesis and the vulnerability hypothesis. Females defended nestlings more often and more vigorously than did males. Given division of labour between sexes and the related reversed sexual dimorphism in size, female Long-eared Owls may be more willing to engage in nest defence simply because they are always nearer eggs and chicks during all breeding stages and are larger/heavier than males; consequently they may allocate more time and energy to this activity. Finally, owls experiencing higher levels of human persecution took smaller risks when defending nests than owls breeding in an undisturbed area.     

Effect of nesting environment on incubation temperature and hatching success of Morelet's crocodile (Crocodylus moreletii) in an urban lake of Southeastern Mexico

Incubation temperature is an important aspect in terms of biological performance among crocodiles, and several controlled experiments have demonstrated a significant relationship between incubation temperature, success in hatching and survival of hatchlings. However, a few studies have tested these relationships in the wild. The objective of this study was to determine the relationship of nest characteristics and environment (hatch year, nest basal area and height, clutch size, distance to shore line, and vegetation cover), to incubation temperature and hatching success among Morelet's crocodile (Crocodylus moreletii). The study was carried out during the nesting seasons of Morelet's crocodile, from 2007 to 2009 in the Laguna de Las Ilusiones, an urban lake located in Villahermosa, Tabasco, Mexico. We physically characterized 18 nests and inserted a temperature data logger in each nest chamber. At the end of the nesting season and prior to hatching, we recovered the crocodile eggs and data loggers and calculated hatching success, under laboratory conditions. We related the environmental variables of the nest with the mean and fluctuation (standard deviation) of nest temperature, using linear models. We also related the environmental variables affecting the nest, to mean nest temperature and fluctuation in incubation temperature and to hatching success, using linear models. Although we found differences in incubation temperature between nests, mean incubation temperature did not differ between years, but there were differences in nest thermal fluctuation between years. The mean incubation temperature for 11 nests (61.1%) was lower than the suggested Female–Male pivotal temperature (producing 50% of each sex) for this species, and all hatchlings obtained were males. There were no differences in clutch size between years, but hatching success varied. Our study indicates that hatching success depends on certain environmental variables and nest conditions to which the eggs are subjected, including season, nest size and clutch size. We also discuss the importance of the fluctuation of incubation temperature on hatching success and sex determination.     

Nest Sanitation as the Evolutionary Background for Egg Ejection Behaviour and the Role of Motivation for Object Removal

Higher interclutch colour variation can evolve under the pressure of brood parasitism to increase the detection of parasitic eggs. Nest sanitation could be a prerequisite for the evolution of anti-parasite defence in terms of egg ejection. In this respect, we used nest sanitation behaviour as a tool to identify: i) motivation and its underlying function and, ii) which features provoke ejection behaviour. Therefore, we experimentally tested whether size, colour or shape may influence ejection behaviour using artificial flat objects. We found a high interclutch variation in egg colouration and egg size in our tree sparrow (Passer montanus) population. Using colour and size we were in fact able to predict clutch affiliation for each egg. Our experiments further revealed the existence of direct anti-parasite behaviours and birds are able to recognise conspecific eggs, since only experimentally-deposited eggs have been removed. Moreover, experiments with different objects revealed that the motivation of tree sparrows to remove experimental objects from their nests was highest during egg laying for objects of varying size, most likely because of parasitism risk at this breeding stage. In contrary, motivation to remove white objects and objects with edges was higher during incubation stage as behavioural patterns connected to hatching started to emerge. The fact that rejection rate of our flat objects was higher than real egg ejection, suggests that egg ejection in tree sparrows and probably more general in small passerines, to be limited by elevated costs to eject eggs with their beaks. The presence of anti-parasite behaviour supports our suggestion that brood parasitism causes variation in egg features, as we have found that tree sparrows can recognise and reject conspecific eggs in their clutch. In conclusion, in tree sparrows it seems that nest sanitation plays a key role in the evolution of the removal of parasitic eggs.     

When do altricial birds reach maximum of their brood defence intensity?

It has been suggested that the brood defence by parents of altricial birds should increase during the breeding attempt until the young depart from the nest. The two proximate hypotheses provide alternative predictions about the peak of brood defence intensity: (1) the vulnerability hypothesis predicts a rapid rise in brood defence after hatching of the chicks, with maximum defence intensity just before fledging and strong decline afterwards; (2) the feedback hypothesis predicts that brood defence intensity will, after a rapid rise, reach a plateau at the end of the nestling period and early after fledging and then slowly decline. I compared brood defence behaviour of altricial meadow pipit (Anthus pratensis) breeding in the Czech Republic during the late nestling stage and during the fledging time. A stuffed stoat (Mustela erminea) was placed 5 m from a meadow pipit nest and the defence behaviour of parents was recorded for 10 min from a hide. Brood defence intensity was higher during the fledgling time than during the late nestling stage, and this trend was more evident in males than in females. Regardless of the proportion of already fledged chicks and those still present in the nest, brood defence did not significantly decrease during the fledgling time in males or females. The results do not agree with the predictions of the vulnerability hypothesis and support the predictions of the feedback hypothesis.     

Are House Wren Troglodytes aedon eggs unusually strong? Test of the predicted effect of intraspecific egg destruction

As a result of opposing selective forces, the external strength of avian eggs should be near some size-specific optimum. However, in certain situations there should be selection on females to lay unusually strong eggs. According to one hypothesis, intraspecific egg destruction should favour increased egg strength as a means of defence against conspecific intruders. This hypothesis predicts that House Wrens Troglodytes aedon , a species well known for its tendency to destroy conspecific clutches, should be under selection for unusually strong eggs. However, the intensity of selection for strong eggs should also be modified by efficacy of nest defence against conspecific intruders in a given species (i.e. efficient nest defence by the breeding pair should weaken selection for unusually strong eggs). The goals of our study were: (1) to establish whether House Wren eggs are stronger than expected for their size; (2) to determine which structural mechanisms are responsible for their unusual strength; and (3) to test a hypothesis that, between wren species, the efficacy of nest defence and the intensity of egg-destroying behaviour affect the intensity of selection for unusually strong eggs. Our results demonstrated that: (1) House Wren eggs are 1.9 times stronger than expected for their size; (2) their unusual strength is achieved mostly by their unusually thick shells; and (3) eggs of the House Wren (extensive paternal nest defence; male egg-destroying behaviour suppressed during incubation) are significantly weaker structurally than eggs of the Marsh Wren Cistothorus palustris (reduced paternal nest defence; male egg-destroying behaviour present throughout incubation). These results are consistent with the hypothesis that the intraspecific egg-destroying behaviour and the efficacy of nest defence by the breeding adults have played a role in the evolution of strength of House Wren eggs.     

Nest-building activity and laying date influence female reproductive investment in magpies: an experimental study

Nest size or nest-building activity has recently been hypothesized to be a postmating sexually selected signal in monogamous birds: females may assess a male's parental quality and willingness to invest in reproduction by his participation in nest building. Females may thus adjust their reproductive effort (i.e. clutch size) not only to their own abilities but also to those of their mates. We investigated whether female magpies, Pica pica, use nest-building activity rather than nest size to adjust their reproductive effort during replacement breeding attempts. After we removed their first clutch, high-quality pairs that built a large nest for the first clutch were more capable of building a replacement nest and females adjusted their clutch size in relation to the time it took to build the nest rather than nest size. We also found support for the hypothesized trade-off between clutch size and egg size in magpies. In replacement clutches females decreased clutch size and increased egg volume, thereby probably improving the survival probability of their offspring in less favourable conditions.Copyright 2002 Published by Elsevier Science Ltd on behalf of The Association for the Study of Animal Behaviour