Ventilation or nest defense—parental care trade-offs in a fish with male care

Brood guarding animals face many critical trade-offs. Sand goby males (Pomatoschistus minutus) build nests with larger openings during low oxygen conditions, presumably to enhance ventilation. However, this may make the nest easier for egg predators to detect and harder for guarding males to defend. Manipulating oxygen level and predator presence (a small crab) for small and large males, we found support for a parental trade-off between fanning and nest defense. An increased fanning activity resulted in less time for guarding. Small males and males in low oxygen showed a higher fanning expenditure than large males and males in high oxygen, but surprisingly, filial cannibalism did not differ between these groups. Males built larger nest openings in low than high oxygen. However, males in both high and low oxygen treatments reduced their nest opening size in the presence of a predator, again indicating an important trade-off between ventilation and nest defense.     

Brood defense and age of young: a test of the vulnerability hypothesis

Summary In many altricial species including the great tit (Parus major) the intensity of brood defense against predators has been shown to increase with the age of the offspring. This effect has been ascribed amongst others to the young becoming more vulnerable as they age (vulnerability hypothesis). In a great tit population suffering heavy losses from brood depredation by the great spotted woodpecker (Dendrocopus major), we rendered first and second broods more vulnerable by artificially enlarging the entrance of the nest hole. Contrary to the vulnerability hypothesis, 16 experimental pairs defended their brood against a dummy great spotted woodpecker less vigorously than did 16 control pairs. Nest concealment behavior potentially compromising active defense was minimized by simultaneous playback of nestling distress calls, thus simulating the act of nest predation. This leaves the brood value hypothesis as an alternative functional explanation of the defense level — age effect. It predicts that parents should defend their brood in proportion to the reproductive value (or some more suitable cohortal equivalent measure) of their offspring. At present, this explanation pertains to one predator species. In first broods, but not in second broods, males defended them more vigorously than did their females. While this parallels previous experiments on brood defense against predators posing a much greater risk to the parents, two functional explanations previously put forward can hardly apply.     

Female nest defense in a coral-reef fish, Dascyllus albisella, with uniparental male care

Intraspecific variation in the patterns of parental care has been observed in a variety of animals; however, the possibility of parental care by a non-caregiving parent of uniparental species has not been thoroughly explored. In the coral-reef damselfish, Dascyllus albisella, only males normally exhibit parental care. In this study, we examined the response of females of this species to egg predators after experimental male removal and an elevated level of egg predation, at two small patch reefs (reefs 1 and 2) in Hawaii. We tested theoretical expectations that a nest was defended only by females which had spawned in the nest, and that larger females had a higher likelihood of defense than smaller females. A nest was defended against egg predators more frequently by females that had spawned in that nest than would be expected by chance. Not all females that had spawned in a given nest participated in defense. There was a positive association between female body length and the likelihood of defense at reef 2, but not at reef 1. Within a set of females that had spawned in the same nest during the same nesting cycle, defending females had larger body lengths than non-defending females at reef 2 but not at reef 1. Lack of association between female size and likelihood of defense at reef 1 was unexpected, but may correlate with the smaller average female size and smaller size differences among females on that reef.     

Risk taking during parental care: a test of three hypotheses applied to the pied flycatcher

According to life-history theory, there will often be a conflict between investment in current versus future reproduction. If a predator appears during breeding, parents must make a compromise between ensuring the growth and survival of offspring (nest defence, feeding and brooding of young), and reducing the risk of predation to ensure their own survival. We model three hypotheses for the outcome of this conflict which are particularly relevant for altricial birds. They are not mutually exclusive, but focus on different costs and benefits. (1) Parental investment is determined by the parents’ own risk of predation. This hypothesis predicts that a lone parent should take smaller risks than a parent that has a mate. (2) Parental investment is related to the reproductive value of the offspring: Parents are predicted to take greater risks for larger broods, larger-sized or older offspring. (3) Finally, we present the new hypothesis that parental investment is related to the harm that offspring would suffer during a period of no parental care (incubation, brooding, feeding). This hypothesis predicts that parents should take greater risks for younger offspring, or for offspring in poorer condition, because the marginal benefit of parental care is largest in such cases. Hence, one may also expect that lone parents should take greater risks than two parents because their offspring are more in need of care. We tested these hypotheses on the pied flycatcher (Ficedula hypoleuca) by presenting a stuffed predator of the parents (a sparrowhawk, Accipiter nisus) close to the nest when parents were feeding the young. Risk taking was measured as the time that elapsed until the first visit to the nest. Most support was found for the ‘‘harm to offspring’’ hypothesis. Previous studies have usually measured the intensity of nest defence against typical nest predators, and have found evidence for the ‘‘reproductive value of offspring’’ hypothesis. However, our model predicts that the importance of the reproductive value of the offspring should decrease relative to the harm that offspring would suffer if they were not cared for when the predator type changes from a nest predator to a predator of adults, and when conditions for breeding turn from good to bad. Received: 13 April 1995/Accepted after revision: 11 March 1996     

Offspring protection by merlin Falco columbarius females; the importance of brood size and expected offspring survival for defense of young

Summary Nest predation was simulated by presenting a stuffed raven close to nests of merlins. This was done to examine the influence of brood size related factors on female defence intensity. The original clutch size did not affect nest defense after hatching, but brood size was important. It determined the attack frequency and, for each brood size level, the proportion of attacking females. When brood sizes were manipulated, the defense intensity increased and decreased, respectively, in relation to the size of the brood. In addition, broods with high future survival (first broods) were defended more vigorously than broods with low future survival (replacement broods). Hence, expected benefits in terms of fledgling production and chick survival seem to be important determinants of female investment in offspring protection. The lower predation rate among females responding with overt aggression to the raven compared to that of less aggressive females suggests that defence of young is beneficial.     

Nest defense and central place foraging: A model and experiment

Summary A graphical model presented here indicates that a nest-defending forager should stay closer to its nest, forage for shorter times per patch, and deliver smaller loads than predicated for delivery rate maximization. The effect is more pronounced farther from the nest, so that if nest defense is especially important, the predator should leave far patches sooner than near ones, and deliver smaller loads from farther away. Moreover, if the attack rate at the nest is increased, the defending forager should move closer and deliver smaller prey.Experimental attacks with stuffed specimens at Gila woodpecker (Melanerpes uropygialis) nests produced the predicted changes in the foraging behavior of males, but not of females.Mated pairs may work as a team to pursue simultaneously two conflicting goals—food delivery and nest protection—both of which affect the survivorship of the young. Sexual dimorphism in monogamous species may result in part from specialization in these roles.     

Offspring reproductive value and nest defense in the magpie (Pica pica)

Summary Magpie (Pica pica) brood defense against a human at the nest was studied in a Mediterranean population with low renesting potential. Variations in two defense measures recorded during 106 trials at 41 different nests were positively correlated with brood age. Ineremental effects due to the number of successive visits to nests by us, brood size, and the time in the breeding season were not significant. Partial correlation analyses showed that visit rate was not an important determinant of nest defense, which thus favors an adaptive explanation of nest defense patterns. Two functional hypotheses to account for the increase in defense intensity with brood age were tested: whether (1) increased parental defense serves to compensate the higher predation risk of older nests or (2) increased parental defense reflects the increasing reproductive value of nestlings as they grow older. Daily mortality and incidende of predation (estimated from contribution of whole-brood losses to total mortality) was higher early in the nestling period, hence providing weak evidence for the assumption on which hypothesis (1) is based. The timing of parental defense intensity did not mirror variations in predation risk for the nest but variations in reproductive value of the brood, as can be estimated from daily mortality, thus supporting hypothesis (2). Magpie parents increased defense intensity in response to premature escaping by almost fully-developed nestlings. Since such a response lowers predation risk for the offspring and increases their probability of survival, this finding supports hypothesis (2), but runs contrary to hypothesis (1). Parents also increased defense in response to play-backs of alarm calls uttered by nestlings during escaping episodes. It is argued that parents should continuously monitor the degree of offspring development in order to assess their reproductive value and that, by alarm calling, chicks honestly make their parents aware of the gain in reproductive value that results from enhancement in locomotory abilities that occur at the end of the nestling period.     

Sex-specific nest defense in house sparrows (Passer domesticus) varies with badge size of males

According to indicator models of sexual selection, females can benefit from choosing males with above average epigamic traits, but empirical evidence for such benefits is scarce. Here, we report results from an experiment with 29 pairs of house sparrows (Passer domesticus) where the intensity of nest defense against a mounted mustelid predator was related to the size of the black throat and breast patch (“badge”) in males. Using principal components analysis (PCA), original response variables of both sexes were reduced to two factors: “Approach” to the predator and “Distant warning”. “Approach”, the more risky behavior, increased from small- through medium- to large-badged males and decreased in their females. Since large-badged males have a higher certainty of paternity (i.e. greater benefits from defense) and may be older and more experienced (i.e. incur lower costs), the most likely explanation for male defense intensity increasing with badge size is an improving benefit/cost ratio. The resulting optimal response of their females and evolutionarily stable participation in joint parental care is illustrated by a graphical model. It shows that females would, indeed, benefit directly from choosing large-badged males. This, however, is no proof of a direct evolutionary tie between badge size and paternal behavior, as assumed by indicator models of sexual selection. It may simply represent a spurious relationship, originating from the correlation of badge size and defense with confidence of paternity. Received: 22 September 1997 / Accepted after revision: 3 November 1997     

Predator-induced female behavior in the absence of male incubation feeding: an experimental study

Parental care plasticity is critical to understanding the ecological and evolutionary influence of nest predation on life history strategies. In birds, incubation imposes a trade-off between the requirements of females (i.e., food) and egg requirements (i.e., heat and protection from predators). However, studies on this topic are rare and usually restricted to species where the male feeds the incubating female, relaxing her incubation costs. Males and females can reduce their activity at the nest to avoid detection by predators. However, females could follow two alternative antipredator strategies: to delay their return to the nest to avoid attracting attention from the potential predator or to return to the nest as soon as possible to enhance nest concealment. In this study, we manipulated the perceived risk of nest predation of incubating common blackbirds (Turdus merula), a species without incubation feeding, to study female behavioral changes induced by nest predation risk. We show experimentally that female blackbirds can reduce their nest visits in the situation with higher nest predation risk. In addition, we confirm that females significantly delay their return to the nest in the presence of a nest predator, contradicting the nest concealment hypothesis. However, our results could be interpreted as a passive antipredator response (to minimize clues given to predators) or as an active antipredator response (to search for predators to expel them from their territories).     

Maternal nest defense reduces egg cannibalism by conspecific females in the maritime earwig <Emphasis Type="Italic">Anisolabis maritima</Emphasis>

Nest predation imposes a major cost to reproductive females, who should therefore take measures to avoid encounters with predators. However, when predators are conspecifics, avoidance can be more difficult and may be a consequence of social or aggregative behaviors. In this study, we measured the consequences of conspecific egg cannibalism on hatching success in the maritime earwig (Anisolabis maritima), which occasionally form aggregations. We hypothesized that conspecific egg cannibalism is a byproduct of aggregation, and that cannibalism rates would increase with aggregation density; however, our results do not support this. We combined field data with a lab experiment to test the effectiveness of maternal nest defense in protecting nests from a conspecific. Nests with a guard had higher hatching success and lower rates of cannibalism than unattended nests in the presence of a conspecific. We also measured body and forcep size to see whether the outcome of contests was determined by relative size. Female guards who were larger relative to the invading conspecific maintained their nest and had higher hatching success than females who were relatively smaller, suggesting that the maritime earwig is under directional selection for larger body and/or forcep size.     

Effects of nest site concealment on hatching success,reproductive success,and paternal behavior of the threespine stickleback,Gasterosteus aculeatus

Summary Male sticklebacks (Gasterosteus aculeatus) actively competed for a limited number of clay flowerpots as nest sites in circular wading pools. Males nesting in pots spawned earlier and more often, had higher mean and lower variance for hatching success (number of fry per gram of estimated clutch weight), and suffered fewer stolen fertilizations, nest raids, and territorial encounters than did males nesting outside pots, and in pools without pots (Table 2). Males nesting in pots had the more even temporal distribution of fanning bouts and interfanning intervals; the durations of fanning bouts and interfanning intervals were less variable for these males (Table 2).In replicate aquaria, one male nested on each side of a glass partition and both males spawned approximately simultaneously. Flowerpots were provided to one, both, or neither male. Males with pots had higher mean hatching success, fewer territorial encounters, and the more even temporal distribution of fanning bouts and interfanning intervals (Table 4).Thus it appears that nest site concealment, in the form of clay flowerpots, affected male hatching success, reproductive success, and parental behavior, even when physical contact between males was prevented. These data suggest that a causal relationship may exist between the paternal fanning regime and the subsequent hatching success. Furthermore, these data suggest that males which nest in high concealment increase their reproductive success, and that females which spawn with these males reduce the variance of their hatching success as well as increase their mean hatching success.     

The costs of male parental care and its evolution in a neotropical frog

Summary Parental care is practiced exclusively by males of the Puerto Rican frog, Eleutherodactylus coqui. Males brood clutches of direct-developing eggs in non-aquatic nest sites and defend eggs against cannibalistic nest intruders. Here, I report on energetic and mating costs incurred by males that provide parental care, and suggest how these proximate costs affect male fitness and the evolution of male parental care in this species. Energetic costs are small for brooding males in comparison to non-brooding, calling males. Brooding males had a higher frequency of empty stomachs and lost small, but significant, fractions of their initial body mass during parental care. Abdominal fat bodies of brooding males during the middle third of parental care were significantly smaller than those of calling males; those of males brooding eggs in earlier or later stages were not different. The mating cost of parental care is greater. Most brooding males cease calling during parental care. However, gravid females are available (i.e., known to mate) on most nights during the principal breeding season; hence non-calling males miss potential opportunities to mate. A mating cost was estimated by calculating nightly mating probabilities for calling males in a plot where nightly calling male densities and daily oviposition schedules were known. On average, a male exhibiting normal calling behavior would be expected to obtain a new mate once every 35.7 days. Hence a brooding male that ceased calling for a 20-day parental care period would miss, on average, 0.56 additional mates. Males that were more successful than average in attracting mates could miss up to 1.63 matings. A marginal value model (Fig. 1) is used to analyze the net effect on male fitness of parental care benefits and costs in E. coqui (Fig. 3). The model indicates that males garner the highest reproductive success by providing care from oviposition through hatching. There is no stage during the pre-hatching period at which a desertion strategy would yield higher reproductive success. In fact, the model suggests that males should provide full parental care even in the face of much higher mating costs than currently obtain in the system.     

Risk-taking by female ducks: intra- and interspecific tests of nest defense theory

We tested several predictions of nest defense theory by observing variation in flushing distance and probability of nest abandonment within and between six species of waterfowl. In these species, only the females incubate eggs and attend offspring. First, we examined whether flushing distance by females varied in relation to clutch size, stage of incubation, and time of season, after controlling for the number of visits made to nests by observers. Revisits by observers appeared to affect flushing distance by females for reasons unrelated to the relative value of the current clutch. We found that as incubation progressed, females allowed observers to approach more closely before flushing from the nest. In some species, females with larger clutches allowed closer approaches to nests before flushing which was also consistent with nest defense theory. In contrast, time of season (Julian date) did not relate to flushing distance for any species. When species were compared, we found that species with moderate to high yearly mortality and high reproductive output per breeding attempt (e.g., northern shoveler and blue-winged teal) were less likely to abandon nesting attempts and exhibited riskier behavior (remained at nests when approached closely by observers) than species that had lower yearly mortality (e.g., mallard). Our results show that flushing distance and patterns of nest abandonment by female ducks conform to several predictions of nest defense theory.Correspondence to: M.R.L. Forbes     

Red-winged blackbird parental investment following brood parasitism by brown-headed cowbirds: is parentage important?

Parental investment by red-winged blackbirds (Agelaius phoeniceus) in response to natural and experi‐mental parasitism by brown-headed cowbirds (Molothrus ater), and in response to freeze-dried, female cowbird mounts presented near redwing nests during the egg-laying period was measured. Two measures of redwing parental investment were used: nest defense effort toward a model predator, and rate of feeding nestlings. There were no significant differences in levels of parental investment among unparasitized nests, naturally parasitized nests, or experimentally parasitized nests. Similarly, parental investment did not differ between redwings that were exposed to the cowbird mount and those that were not exposed to the mount, or among redwings exposed to the cowbird mount at different distances from the nest. This suggests that red-winged blackbirds do not recognize when they have been parasitized, and hence do not associate parasitism with a decrease in their parentage, or that parentage is not an important predictor of parental investment in this species. Received: 24 January 1997 / Accepted after revision: 7 June 1997     

Female choice and the quality of parental care in the great tit Parus major

Summary Previous work on great tits suggested that female mate choice was based on the characteristics of the male rather than the quality of his territory. The aim of this paper was to see whether females were deriving any direct benefits as a result of such choice by comparing male plumage colouration (the size of the central black breast-stripe) with the quality of parental care provided by both members of the pair. Males with large stripes were more likely to defend their broods because their nest attentiveness was higher increasing the chances of predator detection. Males with large stripes produced heavier fledglings primarily as a result of faster growth early in the nestling period. Previous work on great tits has shown that heavier fledglings have a higher survival probability than lighter ones. The results of this study can more easily be explained by differences in parental quality between males rather than as a result of variation in female or territory quality. Therefore, female great tits could increase their reproductive success by pairing with males with a large stripe because such males appear to be better quality parents. This suggests that female choice in the great tit may concern, at least in part, the quality of male parental care.     

Provisioning rules and chick competition in asynchronously hatching common terns (Sterna hirundo)

Interactions between nestling birds and their parents are models for examining parent–offspring communication and sibling competition. Most studies have focused on species where young are restricted to a nest. However, offspring of many species are mobile and fed by parents for an extended period post-hatch. These chicks mobility may provide an opportunity to examine the role of signalling and physical competition on parental feeding decisions. We examined parental provisioning rules in relation to offspring behaviour and hatching order (i.e., competitive ability) in a species with mobile young, the common tern. We determined that about 95% of feedings were directed to the first chick to reach the parent when it landed with food. We developed a probabilistic model to predict the likelihood of a chick reaching the parent first, and thus receiving food. Our model showed that begging intensity, feeding history, and the interaction between begging intensity and relative proximity to the parent best predicted which chick would arrive first. Increased begging was associated with arriving first significantly more when a chick was relatively further from the parent than when it was closer than its siblings. Independently of these factors, larger, earlier-hatched chicks were more likely to be fed than smaller, later-hatched chicks. Additional analyses showed that parents landed closer to more intensively begging chicks, however, increased begging did not explain the advantage of earlier-hatched chicks because begging intensity did not vary with hatching order. Instead, earlier-hatched chicks were more likely to outrun later-hatched siblings and reach the parent first.     

The multidimensionality of behavioural defences against brood parasites: evidence for a behavioural syndrome in magpies?

Studies of antiparasite defences against cuckoo parasites have largely neglected the possibility that behavioural components of host defence may correlate giving rise to a behavioural syndrome. Furthermore, the different contribution of the host’s sex in nest defence has traditionally been disregarded. Here, we studied magpie (Pica pica) mobbing behaviour towards dummies of great spotted cuckoo (Clamator glandarius) and non-harmful hoopoes (Upupa epops) and egg rejection of parasite eggs in a population of colour-banded magpies. We predicted a positive correlation between the intensity of nest defence and egg rejection within each sex and that females respond more intensely than males to the threat of brood parasitism as they undertake incubation. Magpie males, but not females, defended their nests more intensely in those nests in which cuckoo model eggs were rejected. Individual magpies did significantly differ in their baseline level of nest attentiveness; however, there were no individual differences once pair identity was considered. Males and females defended their nests more intensely when it was exposed to the presence of a great spotted cuckoo dummy. Males, but not females, were more prone to appear at their nests, and females, but not males, were more prone to defend more intensely when their nests were challenged by a parasite threat. Our results thus agree with the view that mobbing behaviour and egg rejection in magpies may actually constitute a pseudosyndrome and highlight the necessity to integrate interindividual variation and the sex of the host in studies of the evolution of host defences.     

Hatching asynchrony is constrained by parental nest attendance during laying

Hatching asynchrony is widespread amongst animals, but no consensus has yet emerged as to why asynchronous hatching has evolved. It is generally thought to have adaptive benefits during the raising of dependent young. However, here, we considered an alternative view of hatching asynchrony in birds as a consequence of factors acting at the onset of incubation. We recorded parental nest attendance behaviour during laying using continuous records of nest temperature in herring gulls, Larus argentatus. We tested whether nest attendance during laying was related to individual factors (clutch size and diet) and whether it had consequences on fitness outcomes (hatching spread, incubation period, hatching success and chick survival). Low nest attendance was associated with small clutch size, and independent of clutch size, pairs on a more marine diet had lower nest attendance than pairs on a lower trophic level terrestrial diet, possibly due to higher foraging effort for marine food. Broods hatched more asynchronous where pairs had a lower nest attendance during laying or took longer to complete a clutch and where the last egg took longer to hatch. Low nest attendance was also related to shorter incubation periods, possibly representing a strategy of birds in poor condition to reduce the demand of incubation by reducing the length of incubation. We found that low nest attendance during laying and increasing hatching asynchrony had detrimental effects on hatching success for small eggs laid early in the laying sequence. Increasing hatching asynchrony also had a detrimental effect on the survival of the youngest sibling. In our study population, hatching asynchrony was influenced by a more complex set of factors than simply onset of incubation and appears to be constrained by circumstances at the onset of incubation rather than to be an adaptive strategy. Thus, factors acting both during offspring rearing and at the onset of incubation need to be considered for a better understanding of hatching asynchrony.     

Antipredator responses of California ground squirrels to rattlesnakes and rattling sounds: the roles of sex,reproductive parity,and offspring age in assessment and decision-making rules

California ground squirrels (Spermophilus beecheyi) and northern Pacific rattlesnakes (Crotalus viridus oreganus) have an adversarial relationship. Adults are partially protected by venom resistance and harass rattlesnakes in part to defend their more vulnerable offspring. Larger, warmer snakes are more dangerous than smaller colder snakes, and in escalated conflict squirrels could benefit from risk assessment strategies. Rattlesnakes often rattle at harassing squirrels and rattling sounds produce cues related to body size and temperature. In study 1 we played back rattling sounds from snakes that varied in dangerousness and evaluated the roles of sex and parity in squirrel risk assessment strategies. In general, squirrels tail flagged and stood bipedally more, and were slower to reapproach the playback speaker following playbacks of rattling sounds from more dangerous snakes. In comparison with males and nonmothers, mothers were most responsive to rattling sounds and more sensitive to variation in snake dangerousness. Mothers tail flagged more than males and nonmothers, and this behavior tracked variation in snake dangerousness most closely, perhaps reflecting the effects of snake size and temperature on pup vulnerability. These findings suggest that many aspects of squirrel antisnake behavior are governed by their effects on descendant kin. In study 2 we tested the effects of offspring age on mothers responses to live rattlesnakes and rattling sounds. According to the offspring value hypothesis, mothers should take more risks in defense of older offspring because they are more likely to survive to reproductive age. By contrast, under the offspring vulnerability hypothesis, older offspring are less vulnerable to predators and thus mothers should take fewer risks. Risk-taking, as measured by behaviors that bring the squirrel close to the snakes strike range, was either unaffected by or negatively correlated with offspring age. Thus, our findings suggest that whereas offspring value is unimportant in squirrel antisnake behavior, offspring vulnerability may affect maternal defense. We suggest that offspring vulnerability in mammals, in comparison with birds, may play a larger role in parental defense against predators.Communicated by P.A. BednekoffAn erratum to this article can be found at     

Individual differences in nest defense in the colonial breeding Black-tailed Gulls

Often in colonial seabirds, all colony members are believed to defend against nest predators and experience equal nest predation risk. However, the variation of defense behavior among members and its reproductive consequences are largely unknown. We investigated (1) individual variation in the nest defense of breeding Black-tailed Gulls Larus crassirostris against a natural egg predator, the Jungle Crow Corvus macrorhynchos and (2) how this behavioral variation affects an individual’s own nest predation risk and that of their neighbors. Results were compared between 2 years where crow attack levels were manipulated to average 5 and 22 times normal rates (“low” and “high” predation risk years, respectively) by the placement of varying numbers of artificial nests containing unguarded eggs at the perimeter of the gull colony. In both years, 23–38% of parents, mostly males, showed “aggressive” defense behavior (strikes or chases) against crows and decoys. Other “non-aggressive” gulls showed no defense. In the year of low predation risk, intrusion rates by crows (landing within 0.5 m of an individual gull’s nest) were similar for aggressive and non-aggressive gulls. In the year of high predation risk, however, the rates of intrusion for aggressive gulls (4%) and for non-aggressive gulls with an aggressive neighbor (37%) were significantly lower than for non-aggressive gulls without an aggressive neighbor (76%). These results indicate that aggressive individuals reduce nest predation risk for themselves and conspecific neighbors in a colonially breeding species.