Relative effects of nest size and site on the risk of predation in open nesting passerines

Large nests may incur fitness cost in terms of conspicuousness to predators, but the effect of nest size on predation risk can be confounded by effects of nest site and parental characteristics. I examined relative effects of nest size and placement by experimentally exchanging subsets of inactive nests baited with artificial clutches, among three open-cup nesting passerine species characterized by different nest size, placement and predation rate. The prediction that increasing nest size (original nest replaced by nest of the larger species) would increase predation, while decreasing nest size (replacement by nest of the smaller species) would decrease predation, relative to control (replacement by conspecific nest) was not supported in any species. The prediction that predation should be higher for large nests compared to small ones, even after exchanging nests among species-specific sites, was not supported. Predation rate differed among species (combined site/nest effect) before manipulation, whereas only the effect of nest site was significant after manipulation. This means that predation differed between species-specific nest sites, irrespective of the nest placed at these sites, but not between large (thrush) and small (warbler) nests, irrespective of their placement. Results do not suggest that nest predation selects directionally for smaller nest size. This conclusion could be specific to the study system characterized by high nest densities and high predation rate.     

Evolution of life history traits in Leporidae: a test of nest predation and seasonality hypotheses

Recently, it has been proposed that adult mortality schedules may be responsible for latitudinal patterns of life history variation in passerine birds, whereas nest predation only could explain within latitude patterns. Unfortunately, no independent test has been performed regarding the importance of nest predation with different taxa. In the present study, seasonality and nest predation hypotheses explaining variations in gestation time and litter size in 17 lagomorph species were tested. Among latitude patterns were analysed using the phylogenetic independent contrast method of Felsenstein and within latitude patterns were analysed by the pairwise comparative method. The results obtained indicate that latitudinal patterns observed in both variables are explained by different factors: seasonality for litter size and nest predation for gestation time. Litter size variations within latitudes are also explained by differences in nest predation, supporting previous hypotheses. In conclusion, the present study suggests that, when compared among latitudes, different life history traits (e.g. litter size and gestation time) may be shaped by different selective forces and that the effects of nest predation may be high both within and between latitudes.  © 2006 The Linnean Society of London, Biological Journal of the Linnean Society , 2006, 88 , 603–610.     

Variation in the developmental timing of flight-feather growth in nestling birds

The timing of primary-feather development in relation to growth in body-mass varies considerably between altricial species. This variation relates, at least in part, to differences in nesting habits: species nesting in relatively well-protected nest sites, such as holes, start primary-feather development later than altricial species using open-cup nests. For the latter 'open-nesting' species, the timing of primary-feather development also tends to show an allometric correlation with adult body-size. Since primary-feather development takes longer, rerative to growth in body-mass, in small species than in large ones, these data suggest that, for small species, there will be an important selective advantage in using relatively secure nest sites.     

Predators at bird nests in a northern hardwood forest in New Hampshire

ABSTRACT.   Nest predation is the primary cause of nest failure in most passerine birds, and increases in nest predation associated with anthropogenic habitat disturbance are invoked as explanations for population declines of some bird species. In most cases, however, the identity of the nest predators is not known with certainty. We monitored active bird nests with infrared time-lapse video cameras to determine which nest predators were responsible for depredating bird nests in northern New Hampshire. We monitored 64 nests of 11 bird species during three breeding seasons, and identified seven species of predators during 14 predation events. In addition, we recorded two instances of birds defending nests from predators and, in both cases, these nests were ultimately lost to predation. These results contrast with other studies in terms of the relatively high proportion of nests depredated by raptors and mice, as well as the absence of any predation by snakes. The diverse suite of predators in this and other studies is likely to confound our understanding of patterns of nest predation relative to fragmentation and habitat structure.     

Shade seeking by Common Grackle (Quiscalus quiscula) nestlings at the scale of the nanoclimate

Solar radiation is a major source of heat for open-cup passerine nestlings, and a key variable influencing parental nest site selection. Although temperature, like food, is critical for nestling growth and survival, the use of thermal and insolation gradients when describing passerine nestling orientation and movement within the open-cup nest has not been explored. Our study used the Common Grackle (Quiscalus quiscula) as a model system to directly test the hypothesis that passerine nestlings mitigate thermal extremes behaviourally. Pairs of nestlings were tested in shaded (homogeneous) and exposed (heterogeneous) nests, movements within nests were tracked and nest temperatures recorded. Our results show that nestlings are able to detect and respond to nanoclimate heterogeneity, and can mitigate short-term radiant heat loads through shade-seeking.     

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.     

Understanding avian nest predation: why ornithologists should study snakes

Despite the overriding importance of nest predation for most birds, our understanding of the relationship between birds and their nest predators has been developed largely without reliable information on the identity of the predators. Miniature video cameras placed at nests are changing that situation and in six of eight recent studies of New World passerine birds, snakes were the most important nest predators. Several areas of research stand to gain important insights from understanding more about the snakes that prey on birds' nests. Birds nesting in fragmented habitats often experience increased nest predation. Snakes could be attracted to habitat edges because they are thermally superior habitats, coincidentally increasing predation, or snakes could be attracted directly by greater prey abundance in edges. Birds might reduce predation risk from snakes by nesting in locations inaccessible to snakes or in locations that are thermally inhospitable to snakes, although potentially at some cost to themselves or their young. Nesting birds should also modify their behavior to reduce exposure to visually orienting snakes. Ornithologists incorporating snakes into their ecological or conservation research need to be aware of practical considerations, including sampling difficulties and logistical challenges associated with quantifying snake habitat use.     

Nest predation and nestling growth rate of two lark species in the Negev Desert, Israel

Clutch-size, nestling growth and predation rates on eggs and nestlings in two sympatric alaudids, the Crested Lark Galerida cristata and the Desert Lark Ammomanes deserti, were studied in the Negev desert of Israel. Logistic growth constants were similar for both species, and experimental brood reduction did not accelerate the growth rate of their nestlings. It is suggested that the predation rate on nests of both species has been sufficiently high to select for maximal growth rate of nestlings. Overall probability of predation was 0.85 on a Desert Lark nest and 0.76 on a Crested Lark nest. The smaller clutch-size of the Desert Lark (3.7) may be an adaptation to a higher predation risk, as compared to that of the Crested Lark (4.6) which is more vigilant and nests in more concealed sites.     

Impact of brood parasitism and predation on nest survival of the fan-tailed gerygone in New Caledonia

Predation and brood parasitism are common reasons for nesting failure in passerine species and the additive impact by invasive species is a major conservation concern, particularly on tropical islands. Recognising the relative contribution of the different components of nesting failure rates is important to understand co-evolutionary interactions within brood parasite–host systems. In the remote archipelago of New Caledonia, the fan-tailed gerygone Gerygone flavolateralis is the exclusive host of the brood-parasitic shining bronze-cuckoo Chalcites lucidus. Additionally, invasive rodents also possibly have an impact on breeding success. To estimate the impact of potential nest predators, we 1) video monitored nests to identify predators, 2) estimated the probability of predation based on nest visibility and predator abundance and 3) tested the possibility that the location of experimental nests and lack of odour cues decrease the predation by rodents. In addition, we estimated nest survival rates using data collected in different habitats over the course of eight breeding seasons. Nesting success of fan-tailed gerygones was relatively low and predation was the main cause of nesting failure. We recorded mainly predation by native birds, including the shining bronze-cuckoo, whereas predation by rats was rare. In open habitats predation by cuckoos was much lower than predation by other avian predators. Neither predator activity around nests nor nest visibility influenced the probability of predation. Experimental nests in more accessible locations and containing an odorous bait were more exposed to rodent predation. Apparently, the fan-tailed gerygone has either never been specifically vulnerable to predation by rats or has developed anti-predator adaptations.     

Experiments on clutch size and nest size in passerine birds

Summary Results of experiments on three passerine species suggest that brood size may be constrained by nest size, since the breeding success of pairs provided with large nestcups was greater than that of those provided with small artificial nestcups. These results may have important implications, e.g. to the design of experiments involving manipulation of clutch and brood size. A small nestcup is requisite for successful hatching during the incubation period, but a large one for successful rearing during the nestling period. In nature this difference may select for types of nesting materials that are elastic, such as mosses and lichens. However, experiments showed that such materials rapidly absorb rainwater but only slowly dry out. In addition, because large nests dry out more slowly than small nests, selection will favour small nests among those open-nesting species that have exposed nests. A further possible nest size constraint on open-nesters is nest predation. However, no difference in the predation rate was found in experiments with small and large 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.     

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.     

Testing the importance of nest concealment: does timing matter?

ABSTRACT.   Nest concealment by vegetation is considered an important factor affecting predation rates for many passerines and, therefore, is frequently measured in studies examining nest predation. However, the time when concealment measurements are made may affect the results of such studies, particularly in highly seasonal ecosystems where characteristics of the vegetation later in the breeding period may differ considerably from those at the time of nest-site selection. We used artificial nests baited with quail ( Coturnix sp.) eggs in a highly seasonal tropical dry forest in Jalisco, western Mexico, to test the effects of seasonal change in concealment on nest predation. We placed 40 open-cup, artificial nests in shrubs at the end of the dry season and again at the beginning of the rainy season in 2007, and monitored the fate of the nests and the degree of concealment by vegetation during both periods. Nest concealment was significantly greater during the wet season than during the dry season. The percentage of nests predated was marginally higher during the dry (100%) than the wet (72.5%) season, and daily nest survival was lower during the dry than the wet season. Our results suggest that, in highly seasonal environments such as tropical dry forests, delayed measurement of nest concealment after nest completion rather than during nesting may constitute a significant source of error.     

Foraging behaviour of nest predators at open-cup nests of woodland passerines

Nest predation patterns and processes cannot be understood without studying the behaviour of predators. I videotaped the behaviour of 22 species of predators at 171 depredated nests of 13 passerine species, in woodland in the Czech Republic. About 32% (60/187) of all events occurred during the night; mammals accounted for 95% (57/60) and 22% (28/127) of nocturnal and diurnal predation, respectively. About 67% (57/85) of mammalian predation, but only 3% (3/102) of avian predation, occurred during night. Multiple predations by the same species were detected in at least 7% (6/82) and 42% (37/88) of nests depredated by mammals and birds, respectively. Martens Martes martes/foina took nest content mostly all at once; birds (mainly Jay Garrulus glandarius) revisited partially depredated nest during 1–4 consecutive days. Martens stayed at the depredated nest about five times longer than Jays. Martens spent similar time at nests with eggs and nestling, while Jays stayed about twice longer at nests with eggs. Mammals consumed eggs always at the nest (23/23), but took nestlings away in at least 48% (31/64) cases. Birds took the eggs and nestling away in at least 31% (18/58) and 76% (71/94) cases, respectively. Predator visits to active nests without taking the content, repeated partial predation and revisitation of previously depredated nests suggest an effect of memory on predator’s foraging behaviour.     

Relationship Between Nest Predation Suffered by Hosts and Brown-Headed Cowbird Parasitism: A Comparative Study

There are at least four main hypotheses that may explain how the evolution of host selection by avian brood parasites could be linked to nest predation among their potential hosts. First, selection may have favoured parasite phenotypes discriminating among hosts on the basis of expected nest failure. Second, parasitized nests may be more easily detected by predators and extra costs of parasitism may accelerate the evolution of host defences. Third, selection may have favoured predator phenotypes avoiding parasitized nests because parasitism enhances nest defence. Fourth, female brood parasites may directly or indirectly induce host nesting failures in order to enhance future laying opportunities. We collected data on brood parasitism and nest failure due to predation to test these hypotheses in a comparative approach using North American passerines and their brood parasite, the brown-headed cowbird Molothrus ater. Under the hypotheses 1 or 3 we predicted brood parasitism to be negatively associated with nest predation across species, whereas this relation is expected to be positive if hypotheses 2 or 4 are true. We demonstrate that independent of host suitability, nest location, habitat type, length of the nestling period, body mass and similarity among species due to common ancestry, species experiencing relatively high levels of nest predation suffered lower levels of cowbird parasitism. Our results suggest a previously ignored role for nest predation suffered by hosts on the dynamics of the coevolutionary relationships between hosts and avian brood parasites. Co-ordinating editor: Dr. F. Stuefer     

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.     

Cropland edge,forest succession,and landscape affect shrubland bird nest predation

The effects of habitat edges on nest survival of shrubland birds, many of which have experienced significant declines in the eastern United States, have not been thoroughly studied. In 2007 and 2008, we collected data on nests of 5 shrubland passerine species in 12 early successional forest patches in North Carolina, USA. We used model selection methods to assess the effect of distance to cropland and mature forest edge on nest predation rates and additionally accounted for temporal trends, nest stage, vegetation structure, and landscape context. For nests of all species combined, nest predation decreased with increasing distance to cropland edge, by nearly 50% at 250 m from the cropland edge. Nest predation of all species combined also was higher in patches with taller saplings and less understory vegetation, especially in the second year of our study when trees were 4–6 m tall. Predation of field sparrow (Spizella pusilla) nests was lower in landscapes with higher agricultural landcover. Nest predation risk for shrubland birds appears to be greater near agricultural edges than mature forest edges, and natural forest succession may drive patterns of local extirpation of shrubland birds in early successional forest patches. Thus, we suggest that habitat patches managed for shrubland bird populations should be considerably large or wide (>250 m) when adjacent to crop fields and maintained in structurally diverse early seral stages. © 2011 The Wildlife Society.     

Sources of variation in the nesting success of understory tropical birds

Survival of offspring is a key fitness component and, for birds, the threat of predation on nests is especially influential. Data on rates of nest success from tropical regions are comparatively few, conservation‐relevant, and essential for assessing the validity of models comparing the life histories and behavior or birds across latitudinal gradients. We monitored over 2 000 nests in the lowland forests of central Panama and, using the logistic exposure to model the fate of nests, explored the importance of variation in rate of nest success according to type of nest, height of nests, among years, in early versus late nests, and at different stages of the nest cycle. Analyses of over 1 400 nests for 18 species revealed considerable variation among species in the daily survival rate of nests (range among 18 species=0.91 to 0.98), but nest type and stage of the nesting cycle were generally influential on the probability of nest success. Cavity or enclosed nesters experienced greater nest success than open cup nesters and rates of nest loss were generally greatest in the nestling stage. We found limited evidence that height of nests affected probability of success, but no indication that timing of nesting effort was influential. Despite the occurrence of a severe ENSO event during our sampling, annual variation in nest success was not consistent among species. Interspecific variation in the rates and patterns of nest predation in our study, coupled with reports of high rates of nest loss at temperate latitudes, lead us to question long standing assumptions about latitudinal trends in rates of nest loss. We urge further work to understand the implications of nest predation on the evolutionary ecology of tropical birds.     

Microhabitat structure and avian nest predation risk in an open Argentinean woodland: an experimental study

We studied the effect of the general structure of the nest plant, especially the presence of thorns, and the structural homogeneity of the nest patch, on the vulnerability of nests to predation, using natural and artificial nests. Artificial nests placed in non-thorny plants had a significantly lower predation rate and higher daily survival rate than those in thorny plants. The addition of a ‘thorny microhabitat’ around the immediate proximity of nests placed in non-thorny plants did not have any effect on vulnerability of nests to predation. Conversely, natural nests were located in patches of habitat with a higher density of the species of plant that supported the nest compared to patches selected at random. However, daily survival rate was similar for natural nests placed in patches with a higher or lower density of the species of nest plant in the four bird species analysed. Similarly, survival of artificial nests did not increase with the presence of a higher number of plants similar to the nest plant in the nest patch. Thus, the observed patterns of survival for natural and artificial nests did not seem to support the potential prey-site hypotheses. Birds appeared to be the main nest predators in this ecosystem. Behavioural aspects of the identified predators and habitat structure could explain the lack of effect of thorns and nest patch characteristics on nest survival.     

Contrast in edge vegetation structure modifies the predation risk of natural ground nests in an agricultural landscape

Nest predation risk generally increases nearer forest-field edges in agricultural landscapes. However, few studies test whether differences in edge contrast (i.e. hard versus soft edges based on vegetation structure and height) affect edge-related predation patterns and if such patterns are related to changes in nest conspicuousness between incubation and nestling feeding. Using data on 923 nesting attempts we analyse factors influencing nest predation risk at different edge types in an agricultural landscape of a ground-cavity breeding bird species, the Northern Wheatear (Oenanthe oenanthe). As for many other bird species, nest predation is a major determinant of reproductive success in this migratory passerine. Nest predation risk was higher closer to woodland and crop field edges, but only when these were hard edges in terms of ground vegetation structure (clear contrast between tall vs short ground vegetation). No such edge effect was observed at soft edges where adjacent habitats had tall ground vegetation (crop, ungrazed grassland). This edge effect on nest predation risk was evident during the incubation stage but not the nestling feeding stage. Since wheatear nests are depredated by ground-living animals our results demonstrate: (i) that edge effects depend on edge contrast, (ii) that edge-related nest predation patterns vary across the breeding period probably resulting from changes in parental activity at the nest between the incubation and nestling feeding stage. Edge effects should be put in the context of the nest predator community as illustrated by the elevated nest predation risk at hard but not soft habitat edges when an edge is defined in terms of ground vegetation. These results thus can potentially explain previously observed variations in edge-related nest predation risk.