Using artificial nests to predict nest survival at reintroduction sites

Artificial nests are frequently used to assess factors affecting survival of natural bird nests. We tested the potential for artificial nests to be used in a novel application, the prediction of nest predation rates at potential reintroduction sites where exotic predators are being controlled. We collected artificial nest data from nine sites with different predator control regimes around the North Island of New Zealand, and compared the nest survival rates with those of North Island robin (Petroica longipes) nests at the same sites. Most of the robin populations had been reintroduced in the last 10 years, and were known to vary in nest survival and status (increasing/stable or declining). We derived estimates of robin nest survival for each site based on Stanley estimates of daily survival probabilities and the known incubation and brooding periods of robins. Estimates of artificial nest survival for each site were derived using the known fate model in MARK. We identified the imprints on the clay eggs in the artificial nests, and obtained different estimates of artificial nest survival based on imprints made by different potential predators. We then compared the value of these estimates for predicting natural nest survival, assuming a relationship of the form s = αpβ, where s is natural nest survival and p is artificial nest survival. Artificial nest survival estimates based on imprints made by rats (Rattus spp.) and brushtail possums (Trichosurus vulpecula) were clearly the best predictors (based on AICc), and explained 64% of the variation in robin nest survival among sites. Inclusion of bird imprints in the artificial nest survival estimates substantially reduced their predictive value. We suggest that artificial nests may provide a useful tool for predicting the suitability of potential reintroduction sites for New Zealand forest birds as long as imprints on clay eggs are correctly identified.     

Different nest predator guild associated with egg size in the Patagonian temperate forest

Capsule: Studies of nest predation using artificial nests need to consider the effect of egg size on the types of predator that are detected.

Aims: To estimate the nest predation rate in the Patagonian temperate forest and evaluate the influence of egg size on predator guild.

Methods: On different plant species, we placed 108 nests each containing eggs of either Atlantic Canary Serinus canaria or Common Quail Coturnix coturnix, and a model clay egg of equal size to the real egg. Nest predators were identified from the marks left on the clay eggs or by videos recorded using camera traps.

Results: 86% of the nests were predated. Birds, mainly Chimango Caracara Milvago chimango, were the main nest predators. A marsupial, the Monito del Monte Dromiciops gliroides, and rodents also contributed to nest predation. Nest predation rates were similar for both egg sizes but the nest predator guild was different. Birds and rodents preyed on both eggs but the Monito del Monte consumed mainly small eggs.

Conclusion: Egg size did not influence the rate of nest predation but, instead, affected the nest predator guild. Consequently, in order to avoid underestimating the impacts of small predators, egg size should be considered in studies of nest predation.     

Predation on artificial nests in relation to forest type: contrasting the use of quail and plasticine eggs

Previous studies of avian nest predation have focused on how human-induced changes in the landscape influence the frequency of predation However, natural variation in the abundance of predators due to their choice of habitat can also influence predation rate To determine if predation on artificial nests was influenced by forest stand type, we placed ground and shrub nests containing quail and plasticine eggs in contiguous coniferous, mixedwood and deciduous stands in the southern boreal mixedwood forest of central Canada Nest predators were identified using remotely triggered cameras and marks left in plasticine eggs, while the relative abundance of nest predators such as squirrels and corvids were estimated using acoustic-visual surveys Using the fate of quail eggs to calculate predation rate, we found that predation was significantly higher in coniferous (67%) than in deciduous (17%) or mixedwood (25%) forest, with similar predation on ground (37%) and shrub (29%) nests Using plasticine eggs to calculate predation rate, nests in coniferous forest still suffered higher rates of predation, although predation rates were 15–20% higher, and ground nests suffered significantly higher rates of predation than shrub nests Quail eggs seemed to suffer lower rates of predation because small mammals were unable to penetrate the shell, but could leave marks on plasticine eggs The higher predation rate in coniferous forest was likely caused by higher abundance of red squirrels Tamiasciurus hudsonicus , the presence of fishers Martes pennanti and a simplified understory which may have made it easier for predators to find nests relative to the deciduous and mixedwood forest Plasucine eggs provide new insights into nest predation by identifying predation events by smaller predators such as mice that are missed when using quail eggs     

Nest predation in Australian urban environments and the role of the pied currawong,Strepera graculina

Abstract An experiment, involving 2000 members of the public, determined the identity of nest predators in urban environments. Experimental nests of halved tennis balls covered with coconut fibre and wool were manufactured to resemble the nests of willie wagtails, Rhipidura leucophrys. The identity of predators was determined by analysis of imprints left in artificial eggs made of coloured modelling clay. Sixty-four per cent of nests were preyed upon, with most predation being the result of large birds. Direct observations of predation (n = 134) indicated that pied currawongs were the most common large bird, accounting for 52% of all predation. Predation incidence was higher in gardens with more trees and in which kookaburras, Dacelo novaeguineae, were fed frequently. Among nests placed in trees, nest predation was correlated with nest height. Eggs camouflaged by speckling experienced a similar incidence of predation to plain eggs. This study provides evidence to support the contention that pied currawongs are a major threat to the persistence of small birds in Australian urban environments.     

Rhodamine-B-marked eggs identify individual predators of artificial nests

Investigations of nest predation are often limited by the researchers’ inability to identify nest predators accurately. I tested a chemical bait marker, Rhodamine B (RB), as an indicator of egg predation at artificial ground nests. In a pen trial, the presence of characteristic fluorescent bands in one or more facial vibrissae from all treatment animals confirmed the suitability of RB as a bait marker in the introduced European hedgehog (Erinaceus europaeus). In a field trial in which artificial ground nests were baited with RB-dosed eggs, five of 21 trapped hedgehogs showed evidence of RB ingestion. One animal showed markings indicating two temporally separate predation events. This ability to identify nest predators to species, demographic class, or individual level could lead to more focused control programmes. Other potential uses of this technique include investigation of individual foraging behaviour, calibration of predation rates in artificial nest studies, estimation of the efficacy of poisoned eggs as a control method, and testing for bait or poison uptake by non-target species.     

Do artificial nests reveal relative nest predation risk for real nests?

Present knowledge of the effects of nest predation on spatial distribution, habitat selection and community structure of birds is to a large extent based on results from experiments with artificial nests. Although nest predation risk is likely to differ between artificial and real nests, most previous studies of nest predation using artificial nests have been lacking a proper control. We investigated whether predation rates on artificial nests predicted those on real nests by simultaneously comparing the fate of real and artificial nests (containing quail Coturnix coturnix and plasticine eggs) in 92 territories of the northern wheatear Oenanthe oenanthe in 1996. We also investigated whether risk for artificial nests was related to relative average risk for real nests in these territories (based on data collected two years before and two years after the experiment). Nest predation on artificial nests did predict relative predation risk for real nests only when quail egg depredation was used as the criterion for artificial nest predation. Despite plasticine egg depredation being the most common type of predation it was not associated with predation risk for real nests. Small mice and vole species dominated among cases with only plasticine egg depredation, while predatory mammals and snakes destroyed most quail eggs in artificial nests and most eggs in real wheatear nests. The results suggest that artificial nests may only predict the risk for real nests when the nest predator species are similar among the two types of nest. Furthermore, our data suggest that small mice and vole species rarely depredate nests of mid-sized passerine birds . Our results cast doubt on many previous conclusions based on experiments with artificial nests, since predation risk for such nests is likely to be uncorrelated with risk for real nests due to nest-type-specific differences in nest preying species.     

Predation on artificial and natural nests in the lowland rainforest of Papua New Guinea

Capsule: Although survival of nests was similar between forest fragments and continuous forest, the range of predators differed. Artificial nests provide an under-estimate of nest predation by snakes.

Aims: To estimate the natural nest predation rate in continuous primary forest, compare it with predation rates in forest fragments. To assess the reliability of nest survival rates determined by the use of artificial nests with clay eggs and identify the main nest predators.

Methods: We observed survival of natural nests during the incubation period in continuous primary forest in Papua New Guinea. Some nests were monitored with infrared cameras. We also used artificial nests deployed with clay eggs to identify predators.

Results: There was a predation rate of 50% for natural nests and snakes were major predators of nest contents. Clutch daily survival rates (DSRs) differed among nest types. The DSR of artificial nests (0.977) was not significantly different to that of natural cup nests (0.969). Survival rates of artificial nests were similar in forest fragments and continuous forest. Forest fragments had, however, a higher proportion of avian predators than continuous forest.

Conclusion: Although, we observed similar survival rates in artificial and natural nests, the composition of nest predators was different between natural and artificial nests. Artificial nests were not suitable for estimating the real predation caused by reptiles. Nevertheless, we find that participation of avian nest predators can be estimated correctly with the use of artificial nests.     

Effects of nest-site characteristics and parental activity on cowbird parasitism and nest predation in Brown-and-yellow Marshbirds

ABSTRACT Nest‐site selection and nest defense are strategies for reducing the costs of brood parasitism and nest predation, two selective forces that can influence avian nesting success and fitness. During 2001–2002, we analyzed the effect of nest‐site characteristics, nesting pattern, and parental activity on nest predation and brood parasitism by cowbirds (Molothrus spp.) in a population of Brown‐and‐yellow Marshbirds (Pseudoleistes virescens) in the Buenos Aires province, Argentina. We examined the possible effects of nest detectability, nest accessibility, and nest defense on rates of parasitism and nest predation. We also compared rates of parasitism and nest predation and nest survival time of marshbird nests during the egg stage (active nests) with those of the same nests artificially baited with passerine eggs after young fledged or nests failed (experimental nests). Most nests (45 of 48, or 94%) found during the building or laying stages were parasitized, and 79% suffered at least one egg‐predation event. Cowbirds were responsible for most egg predation, with 82 of 107 (77%) egg‐predation events corresponding to eggs punctured by cowbirds. Nests built in thistles had higher rates of parasitism and egg predation than nests in other plant, probably because cowbirds were most active in the area where thistles were almost the only available nesting substrate. Parasitism rates also tended to increase as the distance to conspecific nests increased, possibly due to cooperative mobbing and parental defense by marshbirds. The proportion of nests discovered by cowbirds was higher for active (95%) than for experimental (29%) nests, suggesting that cowbirds used host parental activity to locate nests. Despite active nest defense, parental activity did not affect either predation rates or nest‐survival time. Thus, although nest defense by Brown‐and‐yellow Marshbirds appears to be based on cooperative group defense, such behavior did not reduce the impact of brood parasites and predators.     

Experimental evidence for edge-related predation in a fragmented agricultural landscape

Abstract This study tested the hypothesis that increased predation of experimental nests occurs close to a forest edge in a fragmented agricultural landscape. Artificial nests and eggs of willie wagtails Rhipidura leucophrys and superb fairy-wrens Malurus cyaneus were used in experiments to assess the extent and nature of predation occurring throughout the known breeding seasons of these species. Predators were identified by the imprints they left in plasticine eggs, and by remote photography. Surveys of avian predators were undertaken to investigate the relationship between predation intensity and predator distribution and abundance. Avian predators accounted for almost all predation for which a predator could be identified (96%). Five of seven predator species photographed attacking wagtail nests were corvids or artamids. Fairy-wren nests suffered relatively low rates of predation (29%) compared to wagtail nests (87%). Increased predation at the habitat edge was recorded for wagtail nests only; predation was correlated with the distribution and abundance of predatory avian species. The different extent and pattern of predation on fairy-wren nests could be explained by problems in detecting predation by mammals, and by possible failure of avian predators to locate the cryptic nests.     

Identifying predators at nests of small birds in a New Zealand forest

Time-lapse video equipment was used to film continuously at nests of two small passerines, the New Zealand Robin Petroica australis and the Tomtit Petroica macrocephala , in an indigenous broadleaf/hardwood forest in central North Island, New Zealand. The nests were illuminated with infrared light to allow night-time observations of predator and parent bird behaviour, and signs left at nests were linked to predator identity. Introduced Ship Rats Rattus rattus and the small native owl or Ruru Ninox novaeseelandiae were filmed preying on eggs or chicks on 12 occasions, and Ship Rats scavenged on eggs on two occasions. Parent birds sometimes altered the signs left at nests after predation, which confused identification of the predator, while Ship Rat scavenger and predator signs were indistinguishable. This suggests that attempts to identify predators from nest signs could be misleading and potentially a widespread problem. Time-lapse video filming with infrared illumination is potentially the least biased method of identifying predators, but it is expensive and so is best used in conjunction with simpler methods. This study found no evidence that filming altered predation rates or that the predators or parent birds reacted strongly to the camera or lights, so we believe that filming is a valuable and safe technique to guide management for the recovery of critically endangered species that are threatened by predators.     

Predators of Greater Sage‐Grouse nests identified by video monitoring

ABSTRACT Nest predation is the primary cause of nest failure for Greater Sage‐Grouse (Centrocercus urophasianus), but the identity of their nest predators is often uncertain. Confirming the identity of these predators may be useful in enhancing management strategies designed to increase nest success. From 2002 to 2005, we monitored 87 Greater Sage‐Grouse nests (camera, N= 55; no camera, N= 32) in northeastern Nevada and south‐central Idaho and identified predators at 17 nests, with Common Ravens (Corvus corax) preying on eggs at 10 nests and American badgers (Taxidea taxis) at seven. Rodents were frequently observed at grouse nests, but did not prey on grouse eggs. Because sign left by ravens and badgers was often indistinguishable following nest predation, identifying nest predators based on egg removal, the presence of egg shells, or other sign was not possible. Most predation occurred when females were on nests. Active nest defense by grouse was rare and always unsuccessful. Continuous video monitoring of Sage‐Grouse nests permitted unambiguous identification of nest predators. Additional monitoring studies could help improve our understanding of the causes of Sage‐Grouse nest failure in the face of land‐use changes in the Intermountain West.     

Predator–prey interactions between the South Polar skua Catharacta maccormicki and Antarctic tern Sterna vittata

Antarctic terns have to co‐exist in a limited space with their major nest predator, the skuas. We conducted artificial nest experiments to evaluate the roles of parental activity, nest location and nest and egg crypsis in this simple predator–prey system. Predation on artificial (inactive) nests was higher in traditional nesting sites than in sites previously not occupied by terns, which suggests that skuas memorized past tern breeding sites. Predation on artificial nests in inactive colonies was higher than in active (defended) colonies. Parental defense reduced predation in colonies to the level observed in artificial nests placed away from colonies. This suggests that communal defense can balance the costs of attracting predators to active colonies. Within colonies, predation was marginally higher on experimental eggs put in real nests than on bare ground. Although it seems that the presence of a nest is costly in terms of increased predation, reductions in nest size might be constrained by the need for protective nest structures and/or balanced by opposing selection on nest size. Predation did not differ markedly between artificial (quail) and real tern eggs. A simultaneous prey choice experiment showed that the observed predation rates reflected egg/nest detectability, rather than discrimination of egg types. In summary, nesting terns probably cannot avoid being detected, and they cannot defend their nest by attending them. Yet, by temporarily leaving the nest, they can defend it through communal predator mobbing, and at the same time, they can benefit from crypsis of unattended nest and eggs.     

Using artificial nests to explore predation by introduced predators inhabiting alpine areas in New Zealand

Abstract

Many bird species endemic to alpine New Zealand are now at critically low densities and restricted in range, making predator‐prey research difficult. We used artificial nests in the Borland Valley, Fiordland National Park, to investigate (1) which introduced species is the most frequent nest predator in the two habitats, (2) whether nest survival differs between habitats, and (3) the utility of artificial nests for guiding conservation management. We used different types of artificial nest in 2 different years and undertook a calibration study of the two types. In 2003, survival of artificial nests containing wax eggs and chicken eggs was high in both habitats. In 2004, survival of artificial nests containing plastilina eggs and chicken eggs was low in both habitats, but was higher in alpine grassland compared with beech forest. Stoats and possums were the most frequent predators (36 and 22% respectively of artificial plastilina nests in alpine grassland and high‐altitude beech forest combined); these percentages did not vary significantly between habitats. Given the low density and sparse distribution of vulnerable species in much of New Zealand, data from artificial nests can be a useful tool for studying predation in these remote and difficult habitats, or at least, preferable to ignorance. However, the type of artificial nest used can strongly affect the rate at which they are destroyed.     

Nest height, nest concealment, and predator type predict nest predation in superb fairy-wrens (Malurus?cyaneus)

Three factors and their interaction effects are increasingly recognized as important determinants of nest predation: nest concealment, nest height, and predator type. The risk of nest predation is predicted to vary across these variables because of nest detectability and accessibility. In general, however, few studies examine how these three variables interact in relation to nest predation, focusing instead on either nest concealment or nest height (whereby predator identity is usually not known). In this study, we examine the role of nest concealment and nest height for nest survival using both artificial and natural nests in the superb fairy-wren (Malurus cyaneus). We indirectly identified potential predators through marks left on artificial eggs and footprints left on tracking tunnels. Predation level at artificial nests was lower than at natural nests, and this could be due to a failure of some nest predators to locate cryptic nests in the absence of cues provided by parental activity. Our results supported the prediction that exposed and concealed nests have different levels of nest predation, which can be explained by variation in predator type. Visual predators were only detected at exposed nests, and survival from visual predators was lower for high nests that were also exposed. However, olfactory predators were detected irrespective of nest height or nest concealment. Because rodents use olfaction to locate nests, this could explain the lack of association between nest concealment and predation outcome at low nests. In addition, rodent footmarks near nests were significantly associated with rodent tooth marks on eggs.     

Predation rate on artificial nests increases with human housing density in suburban habitats

Predation causes most nest failure in birds. Predator communities are likely to vary across a gradient of increasing urbanization, so nest predation also is likely to vary across this gradient. Although predation is thought to decline with increasing urbanization, relatively little is known about variation in predation pressure within strata along an urban gradient and how factors known to affect nest success, such as nest location, interact with urban variables, such as human housing density. Native habitats are frequently fragmented and isolated by suburban residential development, thus we quantified predation rates on artificial nests located in natural oak scrub patches within a suburban matrix in south-central Florida. We examined patterns of predation based on nest location relative to habitat edges, artificial nest weathering treatment, nest shrub height, and human housing density. Over two 18-d trials, we placed a total of 240 nests, each containing a single quail egg and a clay sham, along three roadside transects. Nest predation was not influenced by proximity to edge, nest weathering, or trial date, but was highest at high housing density and lowest at low housing density. The proportion of quail eggs removed from nests increased with human housing density. Birds were the most frequent predators of artificial nests, but the relative frequency of predation by birds or mammals did not differ relative to any of our treatments. Higher rates of nest predation with increasing human housing density within suburban habitats may reflect changes in habitat structure and composition that increase the vulnerability of nests to predation or changes in the composition of the predator community. Our results modify the conclusions of previous studies by suggesting that at scales smaller than the entire urban gradient, nest predation may increase with human housing density, one common measure of urbanization.     

A predator's perspective of nest predation: predation by red squirrels is learned,not incidental

Nest predation has been used to explain aspects of avian ecology ranging from nest site selection to population declines. Many arguments rely on specific assumptions regarding how predators find nests, yet these predatory mechanisms remain largely untested. Here we combine artificial nest experiments with behavioural observations of individual red squirrels Tamiasciurus hudsonicus to differentiate between two common hypotheses: predation is incidental versus learned. Specifically, we tested: 1) whether nest survival could be explained solely by a squirrel's activity patterns or habitat use, as predicted if predation was incidental; or 2) if predation increased as a squirrel gained experience preying on a nest, as predicted if predation was learned. We also monitored squirrel activity after predation to test for evidence of two search mechanisms: area‐restricted searching and use of microhabitat search images. Contrary to incidental predation and in support of learning, squirrels did not find nests faster in areas with high use (e.g. forest edges). Instead, survival of artificial nests was strongly related to a squirrel's prior experience preying on artificial nests. Experience reduced nest survival times by over half and increased predation rates by 150–200%. Squirrels returned to and doubled their activity at the site of a previously preyed on nest. However, neither area‐restricted searching nor microhabitat search images can explain how squirrels located artificial nests more readily with experience. Instead, squirrels likely used cues associated with the nests or eggs themselves. Learning implies that squirrels could be increasingly effective predators as the density or profitability of nests increases. Our results add support to the view that nest predation is complex and broadly influenced (e.g. by predator experience, motivation), and is unlikely to be predicted consistently by simple relationships with predator activity, abundance or habitat.     

Predation by mustelids and rodents on the eggs and chicks of native and introduced birds in Kowhai Bush, New Zealand

Prior to human settlement the endemic New Zealand avifauna evolved in the absence of mammalian predators. Subsequently mustelids, rodents and feral cats have become established and frequently prey on birds and nests. It has been suggested that, because of their evolutionary history, the endemic birds are especially susceptible to such predators. In this paper predation by mustelids and rodents on the eggs and nestlings of eight species of native bird is compared with that on five species of introduced European passerine inhabiting the same lowland forest.
Final outcomes were known for 101 nests of native birds and 48 nests of introduced birds found during three breeding seasons. There was no significant difference between the two groups in frequency of predation. Native birds lost 70-1% of their nests to predators and introduced birds 64-6%. Most predations occurred during the egg stage. Clutch size did not influence frequency of predation, but brood size did for Fantails and introduced birds. Stoats and weasels were responsible for 77-9% of predations on native birds and 77-4% on introduced birds; corresponding percentages for rodents (principally ship rats) were 14-7% and 19-4%. Mustelids destroyed proportionately more nests with chicks than with eggs, whereas rodents did the reverse. Predation on both groups of birds was not influenced by their nesting habitat, the species of tree used for nesting, or the height and position of the nest. The vulnerability to introduced predators of native New Zealand birds is discussed in relation to the historical declines of many species, and also their life-history patterns.     

Egg predation in forest bird communities on islands and mainland

Summary To examine if differences in egg predation rates could explain differences in bird community composition, egg predation was studied in two years on small islands in a South Swedish lake and on the nearby mainland using both natural and artificial nests.In plots with similar vegetation, the combined density of ground- and tree-nesting bird species did not differ between the islands and the mainland. Egg predation rates were similar on islands and the mainland for natural Turdus nests in two years, and for artificial Turdus and Phylloscopus nests. Unmarked and unvisited experimental nests suffered similar rate of egg predation as marked and visited nests. Egg predation rates were higher on natural nests when artificial nests were also put out, increasing the total nest density. Initial egg predation rates in artificial nests were also higher than later when nest density had decreased by 75%.The egg predators involved differed for artificial Phylloscopus nests between the islands and the mainland. Small mammals were apparently responsible for 29% of the predation on the mainland, but none on the islands. Artificial Turdus nests near crow nests suffered from a higher egg predation rate than nests further away from crow nests. Daily survival rates of Turdus nests increased from the laying to the incubation and further to the fledging state.Egg predation can not explain differences in bird community composition between islands and mainland in the present case.     

Why do grebes cover their nests? Laboratory and field tests of two alternative hypotheses

Egg predation is a common feature influencing the reproductive success of open nesting birds. Evolutionary pressure therefore favours building cryptic, inconspicuous nests. However, these antipredatory pressures may be in conflict with thermoregulatory constraints, which select for dry nest material maintaining optimum temperature inside a nest cup during the absence of incubating parents. Here we examined possible trade-offs between nest crypsis and thermoregulation in Little Grebes (Tachybaptus ruficollis), which lay their eggs in floating nests built from wet plant material. As this species regularly covers its eggs with nest material, we experimentally examined (1) the rates of egg predation on covered and uncovered artificial nests and (2) possible thermoregulatory costs from nest covering by comparing temperature and relative humidity changes inside the nest cup. Results revealed that covering clutches is beneficial in terms of deterring predators, because uncovered eggs were more vulnerable to predation. Moreover, covering clutches also had thermoregulatory benefits because the mean temperature and relative humidity inside nest cups covered by dry or wet materials were significantly higher for covered compared to uncovered treatments. Covering clutches in Little Grebes therefore does not pose thermoregulatory costs.     

Testing hypotheses about the function of repeated nest abandonment as a life history strategy in a passerine bird

Nest structures are essential for successful reproduction in most bird species. Nest construction costs time and energy, and most bird species typically build one nest per breeding attempt. Some species, however, build more than one nest, and the reason for this behaviour is often unclear. In the Grey Fantail Rhipidura albiscapa, nest abandonment before egg‐laying is very common. Fantails will build up to seven nests within a breeding season, and pairs abandon up to 71% of their nests before egg‐laying. We describe multiple nest‐building behaviour in the Grey Fantail and test four hypotheses explaining nest abandonment in this species: cryptic depredation, destruction of nests during storm events, and two anti‐predatory responses (construction of decoy nests to confuse predators, and increasing concealment to ‘hide’ nests more effectively). We found support for only one hypothesis – that abandonment is related to nest concealment. Abandoned nests were significantly less concealed than nests that received eggs. Most abandoned nests were not completely built and none received eggs, thus ruling out cryptic predation. Nests were not more likely to be abandoned following storm events. The decoy nest hypothesis was refuted as abandoned nests were constructed at any point during the breeding season and some nests were dismantled and the material used to build the subsequent nest. Thus, Grey Fantails are flexible about nest‐site locations during the nest‐building phase and readily abandon nest locations if they are found to have deficient security.