Differences in Predators of Artificial and Real Songbird Nests: Evidence of Bias in Artificial Nest Studies

Abstract:  In the past two decades, many researchers have used artificial nests to measure relative rates of nest predation. Recent comparisons show that real and artificial nests may not be depredated at the same rates, but no one has examined the mechanisms underlying these patterns. We determined differences in predator-specific predation rates of real and artificial nests. We used video cameras to monitor artificial nests baited with quail and plasticine eggs and Field Sparrow ( Spizella pusilla ) and Indigo Bunting ( Passerina cyanea ) nests in field habitats in central Missouri (U.S.A.). Although daily predation estimates (all predators pooled) were similar between artificial and real nests, predators differed substantially in their depredation of artificial versus real nests. Snakes were the major predator at real nests, and raccoons ( Procyon lotor) were the major predator at artificial nests. We found strong support for models that distinguished predation between two or among three predator groups and between artificial and real nests. There was no snake predation of artificial nests, and the odds of predation of artificial nests was 115–551% (95% confidence interval) and 2–154% of the odds of predation of real nests by mammals and birds, respectively. Artificial nests with plasticine eggs could not be used reliably to identify predators. In several cases plasticine eggs were marked by mice, and raccoons were recorded on video removing the quail egg. Because biases for artificial nests were positive for some predators and negative for other predators (and could be compensating), and potentially existed for all predator groups, conclusions based on artificial nest studies should be suspect even when there is evidence that overall predation rates are similar among real and artificial nests.     

Effects of Exurban Development and Temperature on Bird Species in the Southern Appalachians

Land‐use dynamics and climatic gradients have large effects on many terrestrial systems. Exurban development, one of the fastest growing forms of land use in the United States, may affect wildlife through habitat fragmentation and building presence may alter habitat quality. We studied the effects of residential development and temperature gradients on bird species occurrence at 140 study sites in the southern Appalachian Mountains (North Carolina, U.S.A.) that varied with respect to building density and elevation. We used occupancy models to determine 36 bird species’ associations with building density, forest canopy cover, average daily mean temperature, and an interaction between building density and mean temperature. Responses varied with habitat requirement, breeding range, and migration distance. Building density and mean temperature were both included in the top occupancy models for 19 of 36 species and a building density by temperature interaction was included in models for 8 bird species. As exurban development expands in the southern Appalachians, interior forest species and Neotropical migrants are likely to decline, but shrubland or edge species are not likely to benefit. Overall, effects of building density were greater than those of forest canopy cover. Exurban development had a greater effect on birds at high elevations due to a greater abundance of sensitive forest‐interior species and Neotropical migrants. A warming climate may exacerbate these negative effects. Efectos del Desarrollo Exurbano y de la Temperatura sobre Especies de Aves en las Apalaches del Sur     

Patterns of Nest Predation on Artificial and Natural Nests in Forests

Abstract:  Artificial nest experiments have been used in an attempt to understand patterns of predation affecting natural nests. A growing body of literature suggests that neither relative rates nor patterns of predation are the same for artificial and natural nests. We studied nest predation and daily mortality rates and patterns at real and artificial ground and shrub nests to test the validity of artificial nest experiments. We monitored 1667 artificial and 344 natural nests, over seven trials, in three regions, across 58 sites in Ontario. We controlled for many of the factors thought to be responsible for previously reported differences between predation rates on natural and artificial nests. Although artificial nests in our study resembled natural nests, contained eggs of appropriate size, shape, and color of target bird species, and were placed in similar microhabitats as natural nests, the rates of predation on these nests did not parallel rates on natural nests for any region in terms of absolute rate or pattern. Predation rates on artificial nests did not vary between years, as they tended to for natural nests, and the magnitude of predation pressure on artificial ground nests compared with shrub nests did not show the same pattern as that on natural nests. In general, rates of predation on artificial nests were significantly higher than on natural nests. Our results suggest that conclusions derived from artificial nest studies may be unfounded. Given that many influential ideas in predation theory are based on results of artificial nest experiments, it may be time to redo these experiments with natural nests.     

Blue eggs do not reduce nest predation in the song thrush,Turdus philomelos

Summary Many passerine birds with open cup-shaped nests lay blue or blue-green eggs. In thrushes, blue eggs may be cryptic and provide camouflage by imitating spots of light on green leaves. Alternatively, egg coloration may be selectively neutral because nest predators detect nests and not eggs, or it may be maladaptive because organisms are not always well adapted to their present environment. I evaluated these hypotheses by studying predation on artificial song thrush (Turdus philomelos) nests with quail eggs, painted either white, blue, or spotted (cryptic to a human eye). Corvids were the major nest predators. For concealed as well as exposed nests, I found no differences in the predation rates of nests with white, blue, or spotted eggs. Predators apparently detected the nests, and not the eggs, first. In a second experiment, I placed egg groups without nests in trees to study the effect of color per se. The predation rate of the spotted egg groups was significantly lower than that of the white and blue egg groups, for concealed as well as exposed egg groups. These results suggest that blue eggs in the song thrush are not cryptic but may be selectively neutral or even maladaptive with regard to nest predation.     

Does egg colour affect predation rate on open passerine nests?

The breeding success of many passerines is strongly reduced by egg predation. The adaptive significance of egg crypsis in open nesters is often taken for granted, but visually searching predators may first detect the nest or adult bird and not the eggs. Götmark predicted that selection should favour egg crypsis in the absence of conspicuous nests, whereas birds with conspicuous nests should have non-cryptic eggs. I compared the effect of egg colour treatment (white, blue, brown-spotted) on nest survival (1) among species characterized by different egg coloration, nest size and nest placement, and (2) between relatively well and poorly concealed nests within species. I used artificial nests (n=1,296) and eggs mimicking (except in egg colour) those of the yellowhammer (Emberiza citrinella), blackcap (Sylvia atricapilla) and song thrush (Turdus philomelos). Concurrently, I monitored survival of real nests (n=1,106). Nest survival differed among species, increased with nest concealment and throughout the breeding season, but was not significantly related to egg colour in any species. Nevertheless, the data for the yellowhammer suggest a trend in survival rates across the colour treatments. Brown eggs survived better than white eggs by 11% and 4% in 2 years, but this study had insufficient power to detect effects of this size. The results thus suggest that egg coloration in the song thrush and blackcap (shrub nesters) may be a neutral trait with regard to nest predation, whereas egg crypsis may be an anti-predation feature for the yellowhammer (ground/near-ground nester). The role of predation in the evolution of eggshell colour may vary not only between cavity and open nesters, but also across nest sites within the latter group.     

Patterns of Predation Risk and Survival of Bird Nests in a Chilean Agricultural Landscape

Abstract: We used experimental nests baited with California Quail (  Callipepla californica ) eggs or clay eggs to examine relative risks of nest predation in an agricultural landscape and in two large forest preserves in a south-temperate rainforest in Chile. The most common predators, as identified by marks on clay eggs, were a caracara (   Milvago chimango ), a blackbird ( Curaeus curaeus ), and rodents. Nest losses from predation were similar in large and small forest patches and lower in patches than in extensive forest. In general, predation risk was higher (and nest survival therefore lower) on forest edges than in forest interior, in short-grass pasture than in tall-grass pasture, in narrow corridors than in wide corridors, and on visible nests than on concealed nests. High predation risks in pasture habitat tended to increase the risk of nest predation in adjacent forest edges. For open-cup nesters, the risk of nest predation was relatively high in the present agricultural landscape, indicating that much of the available wooded habitat (  forest edges, narrow corridors) offers poor nesting habitat, although it may be suitable for foraging and traveling. The numerous bird-plant mutualisms in this landscape may be at risk if nesting success of the principal mutualists is consistently low.     

Evidence of an Edge Effect on Avian Nest Success

Abstract:  Habitat fragmentation may modify ecological patterns by increasing the importance of edge effects, including elevating rates of predation on avian nests. Conventional wisdom suggests an increased rate of predation along habitat edges, and previous reviews support this view. These reviews did not apply recent statistical approaches, however, and some were based on a small number of studies. In our meta-analysis of 64 nest-predation experiments, our results supported prior reviews of the general pattern of increased nest predation along habitat edges (  p < 0.01). We separated studies into ecologically relevant categories and found the following patterns: (1) Edge effects were more pronounced in North America and northwestern Europe than in central Europe or Central America. This result may be biased, however, by the different habitats studied in the regions. (2) Marshes and deciduous forests had significant edge effects, whereas edge effects were not apparent in coniferous forests, tropical forests, or fields. (3) Ground and natural nest studies were more likely to exhibit edge effects. (4) Edge effects were detected in studies that used quail eggs and real eggs. (5) Edge effects were not significant when artificial nests were exposed for typical incubation periods, but were significant for shorter exposures. Three alternative hypotheses may explain increased nest predation along edges. The edge-effects hypothesis states that increased nest losses along edges are the result of the habitat discontinuity. The landscape-structure hypothesis states that more fragmented landscapes are more heavily depredated by nest predators. The human-disturbance hypothesis states that near anthropogenic edges increased nest predation is related to human activities. Nest-predation experiments should be placed in a landscape context to reveal differences between the hypotheses.     

Tests of landscape influence: nest predation and brood parasitism in fragmented ecosystems

The effects of landscape fragmentation on nest predation and brood parasitism, the two primary causes of avian reproductive failure, have been difficult to generalize across landscapes, yet few studies have clearly considered the context and spatial scale of fragmentation. Working in two river systems fragmented by agricultural and rural-housing development, we tracked nesting success and brood parasitism in > 2500 bird nests in 38 patches of deciduous riparian woodland. Patches on both river systems were embedded in one of two local contexts (buffered from agriculture by coniferous forest, or adjacent to agriculture), but the abundance of agriculture and human habitation within 1 km of each patch was highly variable. We examined evidence for three models of landscape effects on nest predation based on (1) the relative importance of generalist agricultural nest predators, (2) predators associated with the natural habitats typically removed by agricultural development, or (3) an additive combination of these two predator communities. We found strong support for an additive predation model in which landscape features affect nest predation differently at different spatial scales. Riparian habitat with forest buffers had higher nest predation rates than sites adjacent to agriculture, but nest predation also increased with increasing agriculture in the larger landscape surrounding each site. These results suggest that predators living in remnant woodland buffers, as well as generalist nest predators associated with agriculture, affect nest predation rates, but they appear to respond at different spatial scales. Brood parasitism, in contrast, was unrelated to agricultural abundance on the landscape, but showed a strong nonlinear relationship with farm and house density, indicating a critical point at which increased human habitat causes increased brood parasitism. Accurate predictions regarding landscape effects on nest predation and brood parasitism will require an increased appreciation of the multiple scales at which landscape components influence predator and parasite behavior.     

Evolution of Nesting Height in an Endangered Hawaiian Forest Bird in Response to a Non‐Native Predator

Abstract: The majority of bird extinctions since 1800 have occurred on islands, and non‐native predators have been the greatest threat to the persistence of island birds. Island endemic species often lack life‐history traits and behaviors that reduce the probability of predation and they can become evolutionarily trapped if they are unable to adapt, but few studies have examined the ability of island species to respond to novel predators. The greatest threat to the persistence of the Oahu Elepaio (Chasiempis ibidis), an endangered Hawaiian forest bird, is nest predation by non‐native black rats (Rattus rattus). I examined whether Oahu Elepaio nest placement has changed at the individual and population levels in response to rat predation by measuring nest height and determining whether each nest produced offspring from 1996 to 2011. Average height of Oahu Elepaio nests increased 50% over this 16‐year period, from 7.9 m (SE 1.7) to 12.0 m (SE 1.1). There was no net change in height of sequential nests made by individual birds, which means individual elepaios have not learned to place nests higher. Nests ≤3 m off the ground produced offspring less often, and the proportion of such nests declined over time, which suggests that nest‐building behavior has evolved through natural selection by predation. Nest success increased over time, which may increase the probability of long‐term persistence of the species. Rat control may facilitate the evolution of nesting height by slowing the rate of population decline and providing time for this adaptive response to spread through the population.     

The effects of nesting stage,sex, and type of predator on parental defense by killdeer (Charadrius vociferous): testing models of avian parental defense

Summary Two models predicting the temporal patterns of parental investment in offspring defense over the nesting cycle were tested. The first is based on offspring age, the other on the vulnerability of offspring to predation. Both models make very similar predictions for altricial species after eggs have hatched, i.e., increases in intensity of parental defense until fledging. For precocial species, however, the post-hatching predictions of each model are different: the offspring age model predicts a continued increase in defense intensity, while the vulnerability model predicts a decline. I examined the temporal patterns of parental defense of a precocial shorebird, the killdeer (Charadrius vociferus), and determined which model was supported. Killdeer responses to human and natural predators were observed. Killdeer were less willing to leave the nest, responded most intensely, and displayed closest to a potential predator around hatching. Defense intensity increased from early to late incubation as predicted by the offspring age model. However, after hatching killdeer parental defense declined for both males and females, thus supporting the vulnerability model for this stage. Males and females responded significantly differently to all types of predators. Males took greater risks, remained on the nest longer, defended offspring more intensely, and displayed closer to the predator than females at the approach of a potential predator. Responses to natural predators depended on the type of predator and the approach made by the predator; a greater range of defense behavior was used for predators approaching on the ground compared to aerial predators. In general, killdeer responses to humans were more intense and less variable than their responses to natural predators. This was most likely because the human intruder approached nests and chicks more directly and closer than natural predators.     

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).     

Food and predators affect egg production in song sparrows

Although the possibility that food and predators may interact in limiting avian populations has long been recognized, there have been few attempts to test this experimentally in the field. We conducted a manipulative food addition experiment on the demography of Song Sparrows (Melospiza melodia) across sites that varied in predator abundance, near Victoria, British Columbia, Canada, over three consecutive breeding seasons. We previously showed that food and predators had interactive effects on annual reproductive success (young fledged per female). Here, we report the effects on egg production. Our results show that food limits the total number of eggs laid over the breeding season ("total egg production") and that interactive food and predator effects, including food effects on nest predation, determine how those eggs are "parceled out" into different nests. Food addition alone significantly affected total egg production, and there was no significant interannual variability in this result. At the same time, both food and predators affected the two determinants of total egg production: "clutch number" (total number of clutches laid) and average clutch size. Both clutch number and size were affected by a food x predator x year interaction. Clutch number was lower at low-predator locations because there was less nest predation and thus less renesting. Food addition also significantly reduced nest predation, but there was significant interannual variation in this effect. This interannual variation was responsible for the food x predator x year interactions because the larger the effect of food on nest predation in a given year, the smaller was the effect of food on clutch number; and the smaller the effect of food on clutch number, the larger was the effect of food on clutch size. Potential predator and year effects on total egg production were thus cancelled out by an inverse relationship between clutch number and clutch size. We suggest that combined food and predator effects on demography could be the norm in both birds and mammals.     

Nest-size variation reflecting anti-predator strategies in social spider mites of<Emphasis Type="Italic"> Stigmaeopsis</Emphasis> (Acari: Tetranychidae)

The social spider mites (Acari: Tetranychidae) of Stigmaeopsis weave dense nests on the underside of host leaves. Four species occur on the leaves of bamboo in Japan: Stigmaeopsis longus, S. celarius, S. takahashii and S. saharai. We initially reconfirmed the occurrence of distinct variation in nest size among the species. Based on the hypothesis that this variation plays a role in protecting the spider mites from predators, we looked at the behavior of the natural enemies that occur on the host plants along with members of Stigmaeopsis. We found considerable variation in the ability of nests to protect the spider-mite eggs. The smallest nests protected the eggs against three predators, whereas the largest nests protected the eggs against only one predator species. So, decreases in nest size increased egg defense. Thus we concluded that nest-size variation reflects a strategy for reducing predation.Communicated by D. Gwynne     

Parasitic common goldeneye (<Emphasis Type="Italic">Bucephala clangula</Emphasis>) females lay preferentially in safe neighbourhoods

Nest predation has been suggested as an explanation of the adaptive significance and evolution of conspecific brood parasitism, an alternative reproductive tactic pursued by females in several animal taxa. I used new nest boxes that contained only decoy eggs and were erected on lakes differing in real nest predation risk to test this hypothesis in the common goldeneye (Bucephala clangula), a hole-nesting duck. I used broken eggs to simulate predation risk of the boxes to determine if parasites having no previous experience with the boxes discriminate between seemingly safe and risky nest sites. Parasites laid eggs in the experimental boxes independently of the simulated predation risk, suggesting that they do not use broken eggs or nest disarray as indicators of predation intensity. Parasites preferred experimental boxes on lakes where real nest predation risk was low, supporting the nest predation risk hypothesis. Assuming that females in high risk areas have had experience of nest predation, they may take this into account in selecting host nests.     

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.     

Fieldfare (Turdus pilaris) breeding success in relation to colony size,nest position and association with Merlins (Falco columbarius)

Summary Clutch size, nestling production and breeding success were studied in colonial Fieldfares (Turdus pilaris) in a subalpine birch forest during ten breeding seasons. Reproductive success was highest for central pairs in large colonies; such pairs benefited most from communal defence against nest predators. Fieldfares and Merlins (Falco columbarius) usually bred in association. Fieldfares breeding away from Merlins had lower breeding success than pairs associated with Merlins, which also benefited by reduced nest predation. Fieldfares apparently chose to nest near Merlins, which had already laid eggs when the thrushes started nest-building.     

Independent effects of food and predator-mediated processes on annual fecundity in a songbird

We investigated the relative importance and interaction of ecological processes affecting annual fecundity in birds by simultaneously manipulating food availability and nest predation risk in a small songbird, the Wrentit (Chamaea fasciata). From 2000 to 2002 we provided supplemental food to individual Wrentit territories, and during 2002 we altered nest predation risk by providing supplemental food to their principal predators, Western Scrub-Jays (Aphelocoma californica). These experiments were conducted during a period of high interannual variation in rainfall, with 2002 being one of the driest years on record. Food-supplemented Wrentits in a normal predation environment produced an average of 0.54 more fledglings per year than control pairs over the three breeding seasons. During the feeding plus predation manipulation experiment, Wrentit food supplementation and lowered nest predation risk each independently increased the probability that a Wrentit pair would fledge young; however, the interaction between food supplementation and altered nest predation risk was not significant. Thus, even in an extreme drought year, both food and nest predation had equal but independent effects on reproductive success and annual fecundity. Combining supplemental food with reduced nest predation did not result in a synergistic increase in annual fecundity, primarily because Wrentits did not produce multiple broods. Our results suggest that whether food and predation have additive or synergistic effects on reproductive success depends on the life history of the species and the environment in which they live.     

Potential Impact of Mammalian Nest Predators on Endemic Forest Birds of Western Mauna Kea, Hawaii

I used dummy nest experiments to investigate the role of nest predation by introduced mammals asa significant limiting factor for the endangered Palila ( Loxioides bailleui ) and other endemic birds on the western slope of Mauna Kea. Overall predation rates on dummy nests were extremely low. Rates were comparable to those on actual Palila nests, indicating that dummy nests give a valid representation of the dynamics of nest predation. The black rat ( Rattus rattus ) was the only important predator. Feral cats ( Felis catus ) played only a minor role, and there was no evidence to implicate house mice ( Mus musculus ) as nest predators. Four factors appear to be responsible for the low nest predation rates: (1) only a single species of predator (black rat) is involved; (2) rat densities are extremely low on Mauna Kea; (3) low prey (nest)densities preclude density-dependent predation, and (4) rats have alternative foods that are more abundant and accessible than arboreal bird nests. Since mammalian predation appears unlikely to have a significant impact on the Palila, other factors must be limiting the abundance of this endangered species.     

Forest Fragmentation Increases Nest Predation in the Eurasian Treecreeper

Abstract:  We used long-term breeding data to monitor the influences of fragmentation and habitat composition at different spatial scales on the reproductive success of Eurasian Treecreepers ( Certhia familiaris ) breeding in nest boxes. We collected data from the same forest patches (2.7–65.1 ha in size) during seven breeding seasons. Nest predation varied considerably over the years and was the primary cause of nesting failure (mean annual rate of 21.6 ± 12.8%). Nest predation explained most of the variation in fledgling production during the study period. Landscape-level fragmentation (radius of 500 m from territory center) affected nest predation more than did fragmentation on the territory scale (radius of 200 m from territory center). In general, nest loss due to predation in fragmented landscapes (32.4%) was almost threefold that of less fragmented (12.0%) landscapes. Of the habitat variables, predation rate correlated positively with the density of edges between forest and open land and with the proportion of sapling stands on the spatial scale of 500 m around a nest. In the core area of a territory (radius of 30 m from territory center), a high density of trees increased the frequency of nest predation. Further, a high proportion of agricultural land close to a nest site increased nest losses of treecreepers, probably because of a high degree of mustelid predation. Our results showed that the spatial scale on which we examined nest predation is important and that even within moderately fragmented landscapes it is possible to detect fragmentation-related nest predation.     

The oasis effect: response of birds to exurban development in a southwestern savanna

Ranches are being converted to exurban housing developments in the southwestern United States, with potentially significant but little-studied impacts on biological diversity. We counted birds in grasslands and savannas in southeastern Arizona that were grazed by livestock, embedded in low-density exurban housing developments, or both, or neither. Species richness and bird abundance were higher in exurban neighborhoods than in undeveloped landscapes, independent of livestock grazing. The positive response to development was particularly evident among doves, quail, hummingbirds, aerial insectivores, and some but not all ground-foraging sparrows. Effects of livestock grazing were comparatively minor and mostly involved birds with requirements for tall ground cover or the lack of it. The average rank correlation between counts of individual species and housing density was positive across all transects. However, this relationship disappeared among the exurban transects alone, and bird species richness on the exurban transects was negatively correlated with the number of homes nearby. These results suggest that the positive influence of exurban development on avian abundance and variety was greatest at the lowest housing densities. We attribute the attraction of many birds to exurban development to an oasis effect, in which resources otherwise scarce in arid southwestern environments (shade, nectar, nest sites, and especially water) are relatively abundant around exurban home sites. This finding is consistent with the hypothesis that exurban home sites represented resource supply points inside birds' home ranges otherwise consisting mostly of natural vegetation.